Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 1701–1720 of 55,837 recalls
Recalled Item: Clean-tail Coconut Farm Raise Breaded Butterfly Shrimp Clean Tail (21/25...
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: ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC (SYSCO) Cleantail Recalled...
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: Panko Style Breaded Butterfly Shrimp (16/20 CT per pound) in bulk packaging...
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: Great Value branded and Sea Best branded raw frozen shrimp in bulk packaging...
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: 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: 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.