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. 2,689 recalls have been distributed to Florida in the last 12 months.
Showing 34981–35000 of 55,837 recalls
Recalled Item: UltraSeal XT Plus Clear . The package contains 4x 1.2 Recalled by Ultradent...
The Issue: There was a labeling error with product, UltraSeal XT Plus Clear , Part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...
The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HARVEST SNAPS Recalled by Calbee North America, LLC Due to One lot of black...
The Issue: One lot of black pepper flavored green pea crisps may contain wasabi ranch...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Weck Facial Closure Systems have application in laparoscopic procedures for...
The Issue: The devices wings may become partially detached from the EFx Shield during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (R) DEAD BLOW MALLET Recalled by Smith & Nephew, Inc. Due to The firm...
The Issue: The firm received complaints of cracks in the weld on the head of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Fusion" Oxygenator with Integrated Arterial Filter Recalled by...
The Issue: Medtronic is initiating a voluntary product recall for specific lot numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is Recalled by...
The Issue: The LightCycler¿ 480 algorithm used for the LightMix¿ Zika rRT-PCR Test, EUA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREAST PACK Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...
The Issue: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SET UP PACK Surgical Instrument Tray Recalled by Robert Busse & Co. Inc....
The Issue: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy 4 Implant Recalled by Implant Direct Sybron...
The Issue: The vial cap was mislabeled with the incorrect part number of 855708 but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARPAL TUNNEL PACK Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...
The Issue: Covidien issued a labeling update for the Covidien Devon Light Gloves. Busse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...
The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4C All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cento Romano Grated Cheese Recalled by 4 C Foods, Corp. Due to Potential...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.