Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,715 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,715 in last 12 months

Showing 50615080 of 52,482 recalls

Medical DeviceJuly 24, 2024· ROi CPS LLC

Recalled Item: regard Clinical Packaging Solutions Recalled by ROi CPS LLC Due to Medical...

The Issue: Medical convenience kits were distributed with Merit syringes (manufactured...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 2.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 5.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Cypress Medical Products LLC

Recalled Item: McKesson Syringe 60CC Recalled by Cypress Medical Products LLC Due to...

The Issue: Affected syringes lack FDA clearance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Match Head Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Coarse Diamond Round Recalled by Stryker Corporation Due...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 4.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Precision Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Match Head Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 23, 2024· FDC Limited

Recalled Item: Ciprofloxacin ophthalmic solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: unable to get the solution out of the bottle as the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing