Zimmer Surgical Inc recalls
Every recall we track for Zimmer Surgical Inc — 13 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Zimmer Surgical Inc more than tripled in 2025 (4, up from 1 in 2024).
All FDA recall records for Zimmer Surgical 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 | 0 | 2 | 0 | 2 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 4 | 0 | 4 |
| 2026 (to date) | 0 | 0 | 2 | 0 | 2 |
Most common reasons for Zimmer Surgical Inc recalls
What to do if you have a recalled Zimmer Surgical 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 Surgical Inc recalls
9 shown- Lower riskMedical device
Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors
Zimmer recalls A.T.S 4000 TS Tourniquet Systems Single Hose with CPC Connectors due to potential sterility breach in sealing area, which may cause moderate localized infection if used.
ZimmerJun 9, 2026 - Lower riskMedical device
Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100
Zimmer recalls A.T.S. 3200TS Tourniquet Systems with software version v2.06 or earlier that may freeze in non-English language settings, causing delays when locating an alternate device.
ZimmerDec 24, 2025 - Lower riskMedical device
Zimmer Surgical Inc recalls Zimmer Air Dermatome, Model/Catalog Number: 00880100100
Zimmer Surgical Inc is a leading manufacturer of medical devices and surgical instruments. They are known for their innovative products in the field of orthopedics, neurosurgery, and cardiovascular surgery. Zimmer Surgical Inc offers a wide range of products including surgical instruments, implants, and 3D printing services.
Zimmer Surgical IncNov 24, 2025 - Lower riskMedical device
Zimmer Surgical Inc recalls 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Zimmer Surgical recalls 3:1 Dermacarrier model 00219501300 skin graft carriers due to incorrect ridge ratio (1.5:1 instead of 3:1) which may cause minor tissue damage or unplanned grafts.
Zimmer SurgicalJan 2, 2024 - Lower riskMedical device
Zimmer Surgical Inc recalls Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin
Zimmer recalls 10-pack dermatome blade boxes that may cause skin grafts to be thin and non-uniform, requiring additional harvests. Affected units have specific lot numbers.
ZimmerSep 5, 2023 - Use cautionMedical device
Zimmer Surgical Inc recalls Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No.
Zimmer recalls sterile disposable tourniquet cuffs with dual bladders due to potential leak causing both to inflate/deflate. Affected items have specific lot numbers and item codes.
ZimmerJan 3, 2020 - Lower riskMedical device
Zimmer Surgical Inc recalls Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece, & Alvarado II Base Plate and Foot Piece:
Zimmer Biomet recalls Alvarado Knee Holder Base Plate Assembly and Foot Pieces due to potential foreign material from inadequate cleaning. Affected items have specific item numbers and were sold with all lot codes.
Zimmer BiometApr 16, 2019 - Lower riskMedical device
Zimmer Surgical Inc recalls Zimmer Dermatone AN, Model No. 88710100
Zimmer recalls Dermatone AN surgical devices with model 88710100 that may have loose control bars or width plates, risking uneven graft thickness during skin graft procedures.
ZimmerJun 8, 2018 - Lower riskMedical device
Zimmer Surgical Inc recalls A.T.S. 2200TS Tourniquet Systems, Personalized Pressure. Zimmer Surgical, Inc. Dover, OH 44622 Intended to be used by
Zimmer Surgical recalls A.T.S. 2200TS Tourniquet Systems with updated labels and reduced RF communication distance requirements. Affected units have specific serial numbers and lot numbers listed in the recall notice.
Zimmer SurgicalJul 27, 2017
Zimmer Surgical Inc recall questions
How many recalls has Zimmer Surgical Inc had?
13 recalls from Zimmer Surgical Inc are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Zimmer Surgical Inc recall?
Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors, dated Jun 9, 2026. Every Zimmer Surgical Inc recall is listed on this page, newest first.
Why are Zimmer Surgical Inc products recalled?
The most common reasons on record: The devices may have a misaligned thickness control bar. (2).
What should I do if I have a recalled Zimmer Surgical 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 Surgical 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.