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. 2,736 recalls have been distributed to Wisconsin in the last 12 months.
Showing 1661–1680 of 52,482 recalls
Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...
The Issue: Potential for activation of an abnormal alarm pause.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...
The Issue: Potential for barb non-engagement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...
The Issue: Reverse Shoulder humeral liners have an articular surface position outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartstring III Proximal Seal System Recalled by Maquet Cardiovascular, LLC...
The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frozen AquaStar Breaded Shrimp Recalled by Admiralty Island Fisheries Inc...
The Issue: Product may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Mercado Kroger Cooked Shrimp - Medium - Peeled - Recalled by...
The Issue: Product may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AquaStar Cocktail Shrimp Recalled by Admiralty Island Fisheries Inc dba...
The Issue: Product may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...
The Issue: The device does not bear a unique device identifier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.