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. 2,940 recalls have been distributed to Florida in the last 12 months.
Showing 1301–1320 of 55,837 recalls
Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YO!MAN CUCUMBER (FRESH HUNAN FLAVOR) Recalled by TENGEN USA TRADING CORP Due...
The Issue: Product contains undeclared cyclamates.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: YO!MAN LETTUCE (SPICY FLAVOR) Recalled by TENGEN USA TRADING CORP Due to...
The Issue: Product contains undeclared cyclamates.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OptiWize Health OptiWize Collagen Plus 320 count bottle Recalled by Optiwize...
The Issue: The firm initiated a voluntary recall after NSF testing showed that labeled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sting Relief Swabs Recalled by ACME UNITED CORPORATION Due to Product Mix-up
The Issue: Product Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...
The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Microbiology Data Management System Recalled by Becton...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to Product service...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Instrument Recalled by Becton Dickinson & Co. Due to Product...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dr. Praeger's Recalled by Dr. Praeger's Sensible Foods Inc. Due to Potential...
The Issue: Product was made on equipment that test positive for Listeria .
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bevacizumab 1.75 mg/0.07 mL - 0.25 mL syringe Recalled by RC Outsourcing,...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The...
The Issue: Due to a software error code that crashes during acquisition on patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assay: IMMULITE 2000 Intact PTH Recalled by Siemens Healthcare Diagnostics,...
The Issue: The potential for falsely depressed Intact PTH patient results at the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp Recalled by Admiralty...
The Issue: Shrimp may be contaminated with Cesium-137 (Cs-137).
Recommended Action: Do not consume. Return to store for a refund or discard.