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Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation Recalls

All product recalls associated with Stryker Instruments Div. of Stryker Corporation.

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Recall Summary

Total Recalls

148

Past Year

Class I (Serious)

Most Recent

Jun 2022

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 141–148 of 148 recalls

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1.5 Base Infusion Kit; Product number 501...

The catheter tubing included in the kit may break during removal.

FDAFeb 3, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker PainPump1 2-Site Y-Connector; Product number 500-...

The catheter tubing included in the kit may break during removal.

FDAFeb 3, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker brand Consolidated Operating Room Equipment (CORE...

Potential electrical shock hazard, in that the potential exists for the patient to be exposed to an earth-referenced electrical current.

FDA

1...6 78

Page 8 of 8Next

Aug 5, 2005

• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker brand Intra-Compartmental (STIC) Pressure Monitor...

The pressure indicated may be inaccurate, and this inaccuracy may be not detectable by the user.

FDAJul 22, 2005Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker brand Neptune waste management system, Neptune Ro...

The grounding pin may break inside of the electrical plug, resulting in a shock hazard.

FDAOct 12, 2004Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments, Instruments Div.: Stryker Navigation System - Hip Module Patient Tracker, g...

The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.

FDAJul 14, 2004Nationwide• Stryker Instruments, Instruments Div.

Stryker Instruments, Instruments Div.: Stryker brand OrthoTec pulsed irrigation/suction handpiec...

Product sterility may have been compromised by an inadequate package seal.

FDANov 12, 2003Nationwide• Stryker Instruments, Instruments Div.

Stryker Instruments, Instruments Div.: Stryker Advanced Cement Mixing System Bowl and 180 Gram C...

Non-sterilized product sold as sterile.

FDAJun 1, 2003Nationwide• Stryker Instruments, Instruments Div.