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. 2,616 recalls have been distributed to Florida in the last 12 months.
Showing 45921–45940 of 55,837 recalls
Recalled Item: Human lgG4 Subclass kit for use on the Beckman Coulter Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass Liquid Reagent Kits Human lgG1& lgG2 Antisera Recalled...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MininephThl Human lgG4 Kit Product Code: ZK009.LR This kit is Recalled by...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass Liquid Reagent Kits For use on the Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG4 Subclass Liquid Reagent Kits for use on the Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human lgG Subclass Liquid Reagent Kits for use on the Recalled by The...
The Issue: Customer complaints identified that samples containing extremely high IgG4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...
The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Ingenuity CT system can mislabel the exposure that results in an image in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...
The Issue: Correction due to the detection of a motor sensor failure in the Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specification: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...
The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Injection Recalled by Baxter Healthcare Corp Due to...
The Issue: Correct Labeled Product Mispack: Shipping cartons labeled as containing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xoran MiniCAT X-ray imaging device Recalled by Xoran Technologies, LLC Due...
The Issue: Out of tolerance kVp, Unexposed (black) frames, and Out of tolerance Dose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D'errico perforator drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A zipser clamp is an instrument used to compress reduce Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKenzie enlarging burrs are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gardner-Wells traction tongs are skull tongs for traction used to Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson cranial drill sets (w/ brace and 5 attachments) are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A uterine tenaculum is a hook-like instrument used to seize Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Schoitz weights are manual devices used with Schoitz tonometers and Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.