Stryker Sustainability Solutions recalls
Every recall we track for Stryker Sustainability Solutions — 54 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Stryker Sustainability Solutions peaked in 2018 (8); 54 since 2017. 4% rated “stop using now”.
All FDA recall records for Stryker Sustainability Solutions 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 | 1 | 0 | 1 |
| 2018 | 0 | 3 | 3 | 2 | 8 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 1 | 1 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 1 | 2 | 0 | 3 |
| 2024 | 0 | 0 | 2 | 1 | 3 |
| 2025 | 0 | 1 | 0 | 0 | 1 |
| 2026 (to date) | 2 | 8 | 22 | 2 | 34 |
Most common reasons for Stryker Sustainability Solutions recalls
What to do if you have a recalled Stryker Sustainability Solutions 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 Stryker Sustainability Solutions recalls
23 shown- Use cautionMedical device
Stryker Sustainability Solutions recalls REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM
Stryker recalls XCEL Bladeless Trocar W/Optiview models with specific serial numbers due to potential cracking during use. Affected units may separate, causing injury. Contact Stryker for details.
StrykerAug 19, 2026 - Stop using nowMedical device
Stryker Sustainability Solutions recalls BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
Stryker recalls Bard EP XT Decapolar Steerable Catheters with potential breached sterile barrier. This may cause infection, blood clots, or tissue damage. Stop using immediately if you have the specific lot.
StrykerAug 18, 2026 - Lower riskMedical device
Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
Stryker recalls BARD Dynamic Tip Steerable catheters with incomplete sterile seals that could compromise infection control. Affected units include specific lot numbers and product numbers.
StrykerApr 10, 2026 - Use cautionMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker
Stryker recalls 18" and 24" yellow/red color cuffs with potential detachment at welding connection, causing pressure loss. Affected units include specific serial numbers.
StrykerMar 12, 2026 - Use cautionMedical device
Stryker Sustainability Solutions recalls HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use,
Stryker recalls reprocessed Harmonic Focus Shears with Adaptive Tissue Technology that may become stuck in the 'on' position, causing continuous activation. Affected units have specific lot numbers and were sold for single-use procedures.
StrykerSep 24, 2025 - Lower riskMedical device
Stryker Sustainability Solutions recalls Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A
Stryker recalls disposable 5 lead cable and lead wire systems that may contain reprocessed ECG leads not approved for reuse, potentially causing device malfunction.
StrykerJul 2, 2024 - Lower riskMedical device
Stryker Sustainability Solutions recalls REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Stryker recalls blue 30" tourniquet cuffs labeled as dual port but contain single port. Check packaging for model number 60-7070-0:005 to avoid confusion.
StrykerMay 31, 2024 - UnratedMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions, BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter, REF: D134301, ELECTRODES: 22,
Stryker recalls BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters (REF D134301) due to failing electrophysiology testing requirements. Affected units have specific serial numbers and UDI codes.
Stryker Sustainability SolutionsMay 10, 2024 - Lower riskMedical device
Stryker Sustainability Solutions recalls HoverMatt, 39" W x 78" L, REF: HM39SPU-B
Stryker recalls HoverMatt mattresses with incorrect width that may cause increased skin tears during patient transfers. Affected units were sold between November 28 and December 8, 2022. Contact Stryker for details.
StrykerJun 21, 2023 - Lower riskMedical device
Stryker Sustainability Solutions recalls REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile
Stryker recalls DVT compression foot covers that may be mislabeled or mispackaged. This could lead to incorrect medical use. Affected items have specific lot numbers and sizes.
StrykerApr 14, 2023 - Use cautionMedical device
Stryker Sustainability Solutions recalls Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single
Stryker recalls specific Color Cuff tourniquet cuffs that may tear or have faulty O-rings, causing pressure loss and potential bleeding during medical procedures.
StrykerMar 1, 2023 - Lower riskMedical device
Stryker Sustainability Solutions recalls REF: 5921-018-135, Stryker Color Cuff, 18" (Red), Quick Connect Single Port, Single Bladder
Stryker recalls 18" Red Color Cuff (Quick Connect Single Port) due to mislabeling as single-bladder when it's dual-bladder. This could lead to improper use in medical settings.
StrykerJan 21, 2022 - UnratedMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions REF HARH36 Ethicon Endo-Surgery, Inc. Harmonic ACE +7, Shears with Advanced Hemostasis
Stryker recalls Harmonic ACE +7 Shears with Advanced Hemostasis due to distribution without regulatory clearance. Affected units include specific model and lot numbers. Consumers should contact Stryker for details.
StrykerJan 19, 2021 - Use cautionMedical device
Stryker Sustainability Solutions recalls Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm,
Stryker recalls certain Cardiovascular Reprocessed ViewFlex Xtra ICE Catheters with incorrect expiration dates that may cause sterility breaches or treatment delays. Affected units have a one-year shelf life but are labeled as two years.
StrykerMar 27, 2020 - Lower riskMedical device
Stryker Sustainability Solutions recalls Zimmer Tourniquet Cuff 30" (Blue), PLC Dual Port, Single Bladder, Item Number: 60-7070-105, UDI: 00885825013868,
Stryker recalls blue 30" Zimmer tourniquet cuffs with potential mislabeling that could cause improper use or inadequate limb compression during procedures.
StrykerOct 9, 2019 - Use cautionMedical device
Stryker Sustainability Solutions recalls BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301 Diagnostic electrophysiology (EP) catheters are
Stryker recalls BW Lasso 2515 ANV eco Variable Diagnostic EP Catheters with specific lot codes due to potential EEPROM chip errors when used with CARTO EP Navigation Systems.
Stryker Sustainability SolutionsDec 17, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions LASSO NAV eco Reprocessed Diagnostic EP Catheters designed to obtain
Stryker recalls eco reprocessed electrophysiology catheters (item # D134903) that are not approved for reprocessing, which could lead to improper use.
Stryker Sustainability SolutionsAug 23, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut
Stryker Sustainability Solutions recalls reprocessed arthroscopic shavers with specific catalog numbers that may display incorrect settings or error messages when connected to generators, potentially affecting surgical use.
Stryker Sustainability SolutionsJul 27, 2018 - UnratedMedical device
Stryker Sustainability Solutions recalls Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars12x100mm - Product Usage:
Stryker recalls reprocessed Xcel Bladeless Trocars (H12LP) distributed after a prior recall. These endoscopic surgical tools may be in use at medical facilities. No specific remedy is stated in the recall notice.
StrykerJun 19, 2018 - Use cautionMedical device
Stryker Sustainability Solutions recalls Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage:
Stryker recalls reprocessed HARMONIC Ace+7 shears that may show 'No Instrument Uses Remaining' error code, preventing use. Affected units may need replacement.
StrykerMay 8, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP) Catheter, catalog numbers D135303 and D135304.
Stryker Sustainability Solutions recalls two specific Coronary Sinus Uni-Directional Diagnostic EP Catheter models (D135303/D135304) due to failing non-thrombogenic specifications in testing. The catheters are used for cardiac electrophysiology mapping.
Stryker Sustainability SolutionsMar 29, 2018 - Use cautionMedical device
Stryker Sustainability Solutions recalls Stryker Sustainability Solutions Reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters, Ref D134301,
Stryker recalls reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters due to potential EEPROM chip errors when used with CARTO EP Navigation Systems version 2.3 or higher.
Stryker Sustainability SolutionsJan 2, 2018 - Lower riskMedical device
Stryker Sustainability Solutions recalls 3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector. Intended for
Stry: 3040-VenaFlow Calf Garment (Aircast) was mislabeled as 3010-PL Aircast Pos-Lock Connector. This could cause confusion with a different product intended for DVT prevention. Affected units have UDI: 00885825016661.
StrykerDec 1, 2017
Stryker Sustainability Solutions recall questions
How many recalls has Stryker Sustainability Solutions had?
54 recalls from Stryker Sustainability Solutions are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Stryker Sustainability Solutions recall?
Stryker Sustainability Solutions recalls REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM, dated Aug 19, 2026. Every Stryker Sustainability Solutions recall is listed on this page, newest first.
Why are Stryker Sustainability Solutions products recalled?
The most common reasons on record: Incomplete seals on sterile product (26); Reusable access port system may crack or seperate during use. (6).
What should I do if I have a recalled Stryker Sustainability Solutions 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 Stryker Sustainability Solutions 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.