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Stryker Corporation

Stryker Corporation Recalls

All product recalls associated with Stryker Corporation.

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Recall Summary

Total Recalls

1000

Past Year

731

Class I (Serious)

175

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1061–1080 of 11123 recalls

Stryker iBur 3.0mm Diamond Round, Distal Bend - intended ... (Stryker Corporation) – potential for the product to exhibit ... (2024)

Potential for the product to exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.

FDAJul 24, 2024Nationwide• Stryker Corporation

Stryker iBur 5.0mm Coarse Diamond Round, Distal Bend in... (Stryker Corporation) – potential for the product to exhibit ... (2024)

Potential for the product to exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.

FDAJul 24, 2024Nationwide• Stryker Corporation

Stryker iBur 4.0mm Coarse Diamond Round, Distal Bend - in... (Stryker Corporation) – potential for the product to exhibit ... (2024)

1...52 535455 56...557

Page 54 of 557Next

Potential for the product to exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.

High

FDAJul 24, 2024Nationwide• Stryker Corporation

Karl Storz - Endoskope , REF: 27294AA, Hopkins Telescope ... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27830KA, Nephroscope for MI... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27292AMA, Hopkins Telescope... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27840KA, Nephroscope for MI... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27293AA, Hopkins Telescope ... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27093AA Hopkins Telescope 6... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Karl Storz - Endoskope , REF: 27295AA, Hopkins Telescope ... (Karl Storz Endoscopy) – various medical device product ifus c... (2024)

Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Azelaic Acid Gel (Glenmark) – CGMP Deviation (2024)

CGMP Deviations

Class IIModerate

FDAJul 22, 2024Nationwide• Glenmark Pharmaceuticals Inc., USA

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with In... (Inari Medical Oak Canyon) – laceration hazard (2024)

Laceration Risk

Thrombectomy system catheter instructions for use updated to reduce adverse events due to the following circumstances: 1) Fibrous, firmly adherent, calcified material, or suspected tumor thrombus overloading catheter bag 2) Catheter pulled through internal jugular vein access site or not pulled away from heart; may lead to device entrapment, pulmonary embolism, venous cutdown, abdominal surgery.

FDAJul 19, 2024Nationwide• Inari Medical Oak Canyon

BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure f... (Becton Dickinson & Co.) – may intermittently produce falsely re... (2024)

May intermittently produce falsely resistant results for pyrazinamide (PZA) during susceptibility testing of Mycobacterium tuberculosis isolates.

FDAJul 18, 2024Nationwide• Becton Dickinson & Co.

PE Centrifuge, REF: B36365, a component of the Power Express (Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany) – metal contamination (2024)

The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.

FDAJul 17, 2024Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany

Power Express, REF B90918 (Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany) – metal contamination (2024)

The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.

FDAJul 17, 2024Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany

St. Jerome Cheese (Kenny's Farmhouse) – Listeria risk (2024)

Potential contamination with Listeria monocytogenes

FDAJul 17, 2024AL, GA, ID +4 more• Kenny's Farmhouse Cheese

PE Centrifuge Temperature Controlled, REF: B36366, a comp... (Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany) – metal contamination (2024)

The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.

FDAJul 17, 2024Nationwide• Beckman Coulter Biomedical GmbH Sauerbruchstr. 50 Munchen Germany

Beckman Coulter IRISPEC CA/CB/CC Urine Chemistry Controls... (Beckman Coulter, Inc.) – beckman coulter has become aware of a... (2024)

Beckman Coulter has become aware of an increase in customer complaints for intermittent IRISpec CB negative glucose control failure, resulting in false positive control results when used in conjunction with iChemVELOCITY Urine Chemistry Strips (PNs 800-7204 and 800-7212) on the iChemVELOCITY Analyzer. This issue may delay the reporting of patient results, with a worst-case scenario of a delay in diagnosis or treatment of metabolic disorders, kidney function abnormalities, urinary tract infections, and liver function.

FDAJul 16, 2024Nationwide• Beckman Coulter, Inc.

DxI 9000 Analyzer (Beckman Coulter) – Electric Short Risk (2024)

Ground screws on Dxl 9000 PCB boards may cause electric shorts, leading to smoke and potentially delaying patient results. Smoke also poses a hazard to equipment and users.

FDAJul 12, 2024Nationwide• Beckman Coulter, Inc.