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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

1000

Class I (Serious)

143

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 3161–3180 of 37665 recalls

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.

High

FDAJul 24, 2024Nationwide• Stryker Corporation

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

High

FDAJul 24, 2024Nationwide• Stryker Corporation

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

1...157 158159160 161...1884

Page 159 of 1884Next

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

Moderate

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

2024 STORYTELLER OVERLAND GXV NEXT – storyteller overland, llc (storytelle... (2024)

Storyteller Overland, LLC (Storyteller Overland) is recalling certain 2024 GXV Next vehicles. The Cargo Carrying Capacity listed on the certification label is incorrect, which can allow the vehicle to be overloaded. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other than Passenger Cars."

High

NHTSAJul 23, 2024Nationwide• STORYTELLER OVERLAND

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.

Moderate

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.

Moderate

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

GE Healthcare Centricity Universal Viewer Zero Footprint ... – fire hazard (2024)

Fire/Burn Risk

Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as the original report but at a different time, and only when launched on the following browsers. " Internet Explorer 10 (IE10) " Internet Explorer 11 (IE11) " Firefox.

Moderate

FDAJul 23, 2024Nationwide• GE Healthcare

2024 TEMSA TS35 – fire hazard (2024)

Fire/Burn Risk

Temsa is recalling certain 2024 TS35 vehicles equipped with certain Cummins L9 diesel engines. The remote fuel filter hoses may become separated from the fitting, which can result in a fuel leak and a lack of fuel supply to the engine.

High

NHTSAJul 23, 2024Nationwide• TEMSA

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.

Moderate

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.

Moderate

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.

Moderate

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Ciprofloxacin Ophthalmic Solution (FDC) – Defective Container (2024)

Defective container: unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.

Class IIModerate

FDAJul 23, 2024Nationwide• FDC Limited

VariSoft Infusion Set, Single Use. (Unomedical A/S Osted Aholmvej 1) – specific varisofttm infusion sets wer... (2024)

Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".

Low

FDAJul 23, 2024Nationwide• Unomedical A/S Osted Aholmvej 1

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.

Moderate

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.

Moderate

FDAJul 23, 2024Nationwide• Karl Storz Endoscopy

Desflurane E_Vap.(Saf-T-Fill) used with the A9 Anesthesia... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

V90 electronic vaporizer anesthetic agent output may be higher than the set amount due to a component within the vaporizer causing an incomplete seal in some cases. Should this issue occur, the A9 Anesthesia System will generate alarms associated with abnormal vaporizer output. If the anesthetic concentration is too high, the patient can inhale too much anesthetic agent; the patient may suffer from symptoms such as vertigo and drowsiness after the operation. In severe cases, the patient may suffer from neurological sequelae such as hypomnesia and inattention

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

SlideView VS200 slide viewer, (EVIDENT SCIENTIFIC INC) – a broken fuse inside the laser that w... (2024)

A broken fuse inside the laser that was caused by a short circuit at PIN 4 of the DOOR CTRL. This short circuit was caused by a badly positioned cable that made contact with the housing/frame and caused a short circuit and destroyed the fuse in the laser. This caused the shutter to remain in its most recent state; either in an open or closed position. Once the fuse was destroyed the shutter could not be operated.

Moderate

FDAJul 22, 2024Nationwide• EVIDENT SCIENTIFIC INC

Isoflurane E_Vap.(Safety Filling adapter): used with the ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Sevoflurane E_Vap.(Quik-Fil):used with the A9 Anesthesia ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America

Sevoflurane E_Vap.(Safety Filling adapter) used with the ... (Mindray DS USA, Inc. dba Mindray North America) – v90 electronic vaporizer anesthetic a... (2024)

Moderate

FDAJul 22, 2024CA, GA, KY +6 more• Mindray DS USA, Inc. dba Mindray North America