Zimmer Biomet, Inc. recalls
Every recall we track for Zimmer Biomet, Inc. — 697 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Zimmer Biomet, Inc. peaked in 2018 (294); 697 since 2017.
All FDA recall records for Zimmer Biomet, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 7 | 138 | 32 | 177 |
| 2018 | 0 | 22 | 248 | 24 | 294 |
| 2019 | 0 | 2 | 100 | 20 | 122 |
| 2020 | 0 | 29 | 14 | 61 | 104 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Zimmer Biomet, Inc. recalls
What to do if you have a recalled Zimmer Biomet, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Zimmer Biomet, Inc. recalls
60 shown- Use cautionMedical device
Zimmer Biomet, Inc. recalls Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of
Zimmer Biomet recalls Spinal Rod Cutter (item 00392500200) due to potential fracture during surgical use. Affected units may cause injury if not handled properly.
Zimmer BiometNov 20, 2020 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
Zimmer Biomet recalls Polaris 5.5 Spinal Systems due to risk of spinal screw failure when used with direct current stimulation systems. Affected items include specific model numbers and kits sold in the US.
Zimmer BiometNov 17, 2020 - UnratedMedical device
Zimmer Biomet, Inc. recalls ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Neutral, O.D. Cup with Spacers, 55 mm Item
Zimmer Biomet recalls hip replacement cups due to unconfirmed risk of adverse tissue reactions from residual sterilant. Affected units include specific cup models sold globally. Consumers should contact manufacturer for details.
Zimmer BiometSep 24, 2020 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Dual Mobility Vivacit-E Bearing, Model Number 110031009
Zimmer Biomet recalls Dual Mobility Vivacit-E Bearing model 110031009 due to size mismatch between package label and actual implant. This mismatch risks improper surgical fit.
Zimmer BiometAug 14, 2020 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 5.5X35MM, Item Number 810M5535 - Product Usage: are
Zimmer Biomet recalls certain spinal fixation implants due to reports of screws backing out post-surgery. Affected items have specific model numbers and lot codes. Consumers should contact the company for details.
Zimmer BiometMay 5, 2020 - Lower riskMedical device
Zimmer Biomet, Inc. recalls THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105
Zimmer Biomet recalls THP Hip Plating System with specific item numbers due to potential increased fracture rate and discoloration in packaging.
Zimmer BiometJan 7, 2020 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00
Zimmer Biomet recalls Jamshidi Bone Marrow Aspiration Needles with potential expiration date mismatch between outer and inner labels. Affected lot numbers: 62754464, 62904: 63060634. Contact for remedy.
Zimmer BiometDec 23, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general
Zimmer Biomet recalls ASI 2.0 Calcar Trimmer Shafts with lot numbers 827310, 711160, 203240 due to potential failure to mate with broach during orthopedic surgery.
Zimmer BiometDec 19, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI
Zimmer Biomet recalls Coonrad/Morrey Total Elbow Humeral Assembly model 32-8105-027-04 due to two outer pins instead of one inner and one outer pin, which may cause improper joint function.
Zimmer BiometDec 12, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660
Zimmer Biomet recalls 13mm Orthopedic Bone Saw Cam Assemblies labeled as 14mm due to possible size mismatch. Affected units include specific lot numbers and item numbers. Consumers should contact the manufacturer for details.
Zimmer BiometOct 25, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls BF Humeral Stem, Various Sizes, Item Nos. 00430000606 00430000613 00430000706 00430000713 00430000813 00430000817
Zimmer Biomet recalls certain humeral stems (manufactured before Jan 2014) due to risk of implants adhering to LDPE packaging. Affected items have specific item numbers. No action needed if not in the list.
Zimmer BiometOct 10, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls COMP RVRS Shoulder Baseplates, including Custom Products, Item numbers 115331S 115331 115330S 115330 110040610
Zimmer Biomet is a leading global provider of orthopedic implants and surgical solutions for joint replacement, spinal fusion, and trauma care. We offer innovative products to improve patient outcomes.
Zimmer BiometAug 21, 2019 - UnratedMedical device
Zimmer Biomet, Inc. recalls XP-XP Tibial Tray - Interlok 79 mm Item # 195758
Zimmer Biomet recalls XP-XP Tibial Tray - Interlok 79mm (Item #195758) due to locking bar not fully engaging, which may cause instability during surgery. Affected units have specific lot numbers listed in the recall.
Zimmer BiometAug 15, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
Zimmer Biomet recalls ASI 2.0 Calcar Trimmer Shafts (model 110032331) due to risk of improper mating with Calcar Planar Shaft instruments. Affected units include specific lots.
Zimmer BiometAug 6, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812
Zimmer Biomet recalls Orthopedic Salvage System Hybrid Poly Tibia Item #151812 due to potential ineffective cleaning processes. Affected products were distributed from June 2016 to February 2019.
Zimmer BiometJul 2, 2019 - UnratedMedical device
Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
Zimmer Biomet recalls specific models of Comprehensive Reverse Shoulder Instrument Case (Outer Case Vault Only) due to inadequate sterilization validation. Affected units may not be properly sterilized, posing infection risks during surgical procedures.
Zimmer BiometJun 10, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Ultra-Drive Irrigation Tubing Assembly, Reference Number 423834 - Product Usage: Item used with the UltraDrive System
Zimmer Biomet recalls Ultra-Drive Irrigation Tubing Assembly (lot numbers listed) due to insufficient shelf life data supporting 10-year label. Consumers should check if their product has listed lot numbers and contact for details.
Zimmer BiometJun 4, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are
Zimmer Biomet recalls DVR Crosslock ePAK Screw Drivers with model 212000002 due to potential weak sterile packaging seals. Affected units include specific lot numbers from 2018-2023. Consumers should check their product for the model and lot numbers listed.
Zimmer BiometMay 28, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421060 Phase 3 Femoral Drill
Zimmer Biomet recalls specific partial knee drill guides due to potential corrosion from incorrect raw materials. Affected items include Lot Numbers ZB160601 to ZB170601. Contact for return instructions.
Zimmer BiometApr 18, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Mobi-C 14mm Distraction Screw, Quick Start. Intended for cervical intervertebral disc replacement. Item Number:
Zimmer Biomet recalls Mobi-C 14mm Distraction Screws with a mislabeled 12mm part on packaging. This could lead to using the wrong size screw during cervical spine surgery. Affected units have item number 0024-LDR.
Zimmer BiometApr 1, 2019 - Use cautionMedical device
Zimmer Biomet, Inc. recalls T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Biomet Headless Compression Screws and Twist-Off
Zimmer Biomet recalls T7 Driver Cannulated AO (Part 110018531) due to potential fracture, bending, or shearing of the driver. Affected lot numbers include 13422A through 15310B. Consumers should check their product details.
Zimmer BiometMar 28, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile Titanium. Accessory to total hip implant Item
Zimmer Biomet recalls hip screws that may be mislabeled as 20mm when they are 30mm, risking surgical errors. Affected units include specific lot numbers. Contact for replacement.
Zimmer BiometMar 1, 2019 - UnratedMedical device
Zimmer Biomet, Inc. recalls Biomet Small Diameter Cement Plug Inserter-Sterile, single-use accessory instrumentation to be used during surgical
Zimmer Biomet recalls sterile surgical cement plug inserters due to inadequate sterilization validation. Affected items were sold for surgical procedures. Consumers should contact the company for details.
Zimmer BiometFeb 28, 2019 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
Zimmer Biomet recalls Vanguard Knee System Series-A Standard Patella sizes 31mm (Item 184764) due to potential size mismatch with label. Affected patients should contact for details.
Zimmer BiometDec 21, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet
Zimmer Biomet recalls specific model of shoulder replacement implants due to potential packaging without taper adapter. Affected units may need verification and action.
Zimmer BiometDec 21, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants
Zimmer Biomet recalls specific caddy models for potential silicone shedding during cleaning and sterilization. Affected units include lot numbers 453392 to 512868. Consumers should contact the company for details.
Zimmer BiometNov 28, 2018 - UnratedMedical device
Zimmer Biomet, Inc. recalls Biomet DVR Crosslock Screws- 2.7mm x 20mm, Sterile ITEM 131827120 Product Usage: The system is intended for
Zimmer Biomet recalls 2.7mm x 20mm crosslock screws with incorrect sizes (18mm instead of 20mm) that could cause improper bone fixation during surgery. Affected items have specific lot numbers.
Zimmer BiometNov 20, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Lineum 4.35mm x 28mm Translation Screw, Model No. 14-524728 The Lineum OCT Spine System is intended to provide
Zimmer Biomet recalls Lineum 4.35mm x 28mm Translation Screw (Model 14-524728) due to incorrect 24mm marking on tulip head. This could lead to improper spinal alignment during surgery. Affected patients should contact manufacturer for details.
Zimmer BiometNov 14, 2018 - UnratedMedical device
Zimmer Biomet, Inc. recalls NexGen¿ Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw Item Number: 00599003523
Zimmer Biomet recalls NexGen Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw (Item #00599003523) due to missing screw in package. Affected patients should contact manufacturer for details.
Zimmer BiometOct 31, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562
Zimmer Biomet recalls 20mm Compress Device Short Anchor Plug With Drill Set due to potential metal burrs causing improper implant insertion. Affected units may require replacement to prevent complications during surgery.
Zimmer BiometOct 24, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
Zimmer Biomet recalls Vanguard Knee System -PS Open Box Femoral Left 62.5mm (Item 183126) due to mismatched labels between outer carton and inner sterile packaging.
Zimmer BiometOct 22, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2237-033-00
Zimmer Biomet recalls certain intramedullary guide wires due to potential sterility compromise from creases in the sealing area. Affected items have item number 47-2237-033-00 and expire before September 30, 2023.
Zimmer BiometOct 22, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer Compress Devices and Instruments: Item Number/Item Description 178350 Compress Device Anti-Rotation Spindle
Zimmer Biomet recalls specific compress devices and instruments due to a correction in surgical technique instructions for anti-rotation pins. Affected items include various spindle and sleeve models.
Zimmer BiometOct 12, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Porous Stem, Item No. 150394
Zimmer Biomet recalls specific Orthopedic Salvage System (OSS) porous stems due to potential surgery extension risk if replacement parts are unavailable. Affected patients should contact the company for details.
Zimmer BiometOct 10, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail 125 Deg 12x165mm, Item Number 816712165 The Affixus Hip Fracture Nail System, comprised of
Zimmer Biomet recalls Affixus Hip Fract: Set screw cannot advance or reverse, potentially causing improper fracture stabilization.
Zimmer BiometOct 2, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls StageOne Hip, Models 431207 & 431209Usage: Product Usage: The single-use cement spacer molds are sterile disposables
Zimmer Biomet recalls StageOne Hip cement spacer molds 431207 and 431209 due to potential mixing of 43mm and 51mm molds. These sterile medical devices could cause incorrect joint fitting if used improperly.
Zimmer BiometSep 21, 2018 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Biomet Microfixation RapidFlap System 16MM RapidFlap SpinDown Clamp, 12 Pack Ref Number: 75-1030-12 Used for the
Zimmer Biomet recalls 12-pack of 16MM RapidFlap SpinDown Clamps due to incorrect assembly, which may cause injury during surgery. Affected units have lot expiry before 09/18/2023.
Zimmer BiometAug 22, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus Hip Fracture Nail Right 130 11 mm x 340 mm, Item Number 814511340 Product Usage: Intended for the fixation of
Zimmer Biomet recalls Affixus Hip Fracture Nails with lot number 369640 due to sterile packaging opening during surgery. Affected patients should contact the company for details.
Zimmer BiometAug 8, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone
Zimmer Biomet recalls certain long flex drill bits due to incorrect expiration date on labels. This may lead to using expired medical devices. Affected items have specific lot numbers.
Zimmer BiometAug 3, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total
Zimmer Biomet recalls Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment (Model 185224) due to one bolt missing from sterile package. This could cause improper implant fixation.
Zimmer BiometAug 2, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer Natural Nail Tibial Nail - Yellow 8.3mm, Model Number 47249534008 Product Usage - The Zimmer Natural Nail System
Zimmer Biomet recalls Yellow 8.3mm Tibial Nails (Model 47249534008) that are actually 12mm. This size error may cause improper bone fixation during fracture treatment.
Zimmer BiometJul 30, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Gentle Thread PLGA Full Thread Interference Screw, 10x30mm, Item Number 905629
Zimmer Biomet recalls specific PLGA screws (item 905629) that may have been mixed with other models, posing a risk of incorrect use in medical procedures.
Zimmer BiometJul 20, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 440 mm, Item Number: 814309440
Zimmer Biomet recalls specific hip fracture nail models due to set screw failure. Affected items may not advance or reverse properly, potentially causing improper fixation.
Zimmer BiometJul 17, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Peg Fully Threaded, Locking, 2.5mm x 10mm, Item Number 131212610 Orthopedic device used for stabilization and fixation
Zimmer Biomet recalls Peg Fully Threaded, Locking 2. 5mm x 10mm units due to a 22mm threaded peg found in some packages. This could cause improper fixation of bone fragments.
Zimmer BiometJul 12, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Persona Partial Knee System Spacer Block Alignment Tower, Item No. 42-5399-006-35 Product Usage: Intended to aid in
Zimmer Biomet recalls Persona Partial Knee System Spacer Block Alignment Tower (Item No. 42-5399-0:35) due to potential surgical delays under 30 minutes. This device is used in knee surgery preparation.
Zimmer BiometJun 22, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Connecting Bolt, Model 14-442093
Zimmer Biomet recalls Connecting Bolt Model 14-442093 due to potential decrease in fatigue strength leading to fracture. Affected users should contact the company for details.
Zimmer BiometJun 18, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.
Zimmer Biomet recalls ARCOS Modular Revision Hip System item 11-300: Potential for extended surgery time if components are mixed.
Zimmer BiometJun 8, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 13.5; 00-7713-013-00
Zimmer Biomet recalls M/L Taper Hip Prostheses with Kinective Technology (size 13.5) made before Oct 2015 due to potential black residue in polyethylene bags. This residue may delay surgery or cause wear during implant use.
Zimmer BiometMay 30, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The
Zimmer Biomet recalls Vanguard Complete Knee Systems with specific model numbers due to potential mix-up of 12mm and 14mm tibial bearings, which could lead to extended surgery time.
Zimmer BiometMay 24, 2018 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01)
Zimmer Biomet recalls 75mm tibial tray implants that may be mislabeled as 79mm, causing surgery delays or revision. Affected items have specific UDI codes.
Zimmer BiometMay 18, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls G-PIN 2.8BL 3.2PL 98CM 2PK; 467260 Intended to be used as a guide pin for insertion of implants (cannulated screws
Zimmer Biomet recalls certain G-PIN guide wires due to potential sterile barrier breaches causing infection risk. Affected items have specific model numbers and were sold in the US. Consumers should contact the company for details.
Zimmer BiometMay 16, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replacement procedures.
Zimmer Biomet recalls Vanguard Knee System PS Tibial Bearing (Part 183621) due to incorrect size labeling in the label master file, which could lead to improper knee joint replacement procedures.
Zimmer BiometMay 11, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Lactosorb RapidFlap, bone plate, Model No. 915-0020 The RapidFlap LS Cranial Fixation System is indicated for use in
Zimmer Biomet recalls Lactosorb RapidFlap bone plate model 915-0020 with excessive chamfer on threading. This may cause improper fit during cranial surgery. Affected lots listed in the recall notice.
Zimmer BiometApr 5, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The
Zimmer Biomet recalls Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar Model CP260600 due to potential dry blast irregularity in locking collar screws.
Zimmer BiometApr 3, 2018 - Use cautionMedical device
Zimmer Biomet, Inc. recalls Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented
Zimmer Biomet recalls hip implants with potentially mixed head sizes, risking dislocation during surgery. Affected patients should contact the company for details.
Zimmer BiometApr 2, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is
Zimmer Biomet recalls specific segmental system proximal femoral components for possible debris in the hole during machining, which may not have been fully cleaned. This affects certain surgical implants used in complex bone repair cases.
Zimmer BiometMar 29, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Gentle Threads, Interference Screw; Model No. 905604, for soft tissue reattachment procedures in the ankle/foot and
Zimmer Biomet recalls specific lots of Gentle Threads Interference Screw (Model 905604) due to potential infection from overexposure during EtO sterilization.
Zimmer BiometMar 28, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter, 70 cm Length; Item Number: 00-2255-026-00
Zimmer Biomet recalls specific humeral guide wire models due to potential failure of sterile packaging seals. This could lead to contamination risks during medical procedures. Affected units include lot numbers 63733046, 63758: 77006554.
Zimmer BiometMar 26, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Phoenix Nail System, intended for use with an intramedullary nail system for alignment, stabilization and fixation of
Zimmer Biomet recalls certain Phoenix Tibia Nail 3.5mm Inserter instruments manufactured before March 30, 2017 due to reports of fracturing and remaining in the device implant after surgery.
Zimmer BiometMar 12, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Zimmer M/L Taper Hip Prosthesis, 7711 Series, Femoral Stem 12/14 Neck Taper Plasma Sprayed Press-Fit Cementless Size 4
Zimmer recalls certain hip implants that contain a smaller size than labeled, which could lead to improper fit and complications. Affected packages have specific part and lot numbers.
ZimmerMar 1, 2018
Zimmer Biomet, Inc. recall questions
How many recalls has Zimmer Biomet, Inc. had?
697 recalls from Zimmer Biomet, Inc. are on record with U.S. safety agencies, from 2017–2020.
What is the most recent Zimmer Biomet, Inc. recall?
Zimmer Biomet, Inc. recalls Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of, dated Nov 20, 2020. Every Zimmer Biomet, Inc. recall is listed on this page, newest first.
Why are Zimmer Biomet, Inc. products recalled?
The most common reasons on record: The locking bar not fully engaging (35); Potential failure of sterile packaging seal. (12); Cleaning processes potentially being ineffective (6); There is a potential for weak seals of the sterile packaging. (3).
What should I do if I have a recalled Zimmer Biomet, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Zimmer Biomet, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.