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. 2,698 recalls have been distributed to Florida in the last 12 months.
Showing 34101–34120 of 55,837 recalls
Recalled Item: CycloSPORINE Capsules Recalled by Amerisource Health Services Due to Failed...
The Issue: Failed Impurities/Degradations Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-PACK TPOAb CONTROL SET Recalled by Tosoh Bioscience, Inc. Due to The...
The Issue: The label contains two different methodologies. Quality Control values for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK TgAb CONTROL SET Recalled by Tosoh Bioscience, Inc. Due to The...
The Issue: The label contains two different methodologies. Quality Control values for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....
The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Ophthalmic Solution Recalled by Actavis Inc Due to Failed...
The Issue: Failed Impurities/ Degradation Specifications: OOS for related compound...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide 2.5 mg ER Tablets Recalled by RemedyRepack Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xanthium & Siler Combo (Bi Yan Pian) DIETARY SUPPLEMENT Recalled by Kingsway...
The Issue: Presence of Ephedrae Herba (ma huang), a FDA Banned Ephedra Alkaloid
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mahatma Broccoli & Cheese Rice Recalled by Riviana International, Inc Due to...
The Issue: Foreign Material (Metal) in pouched Rice Mixes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: (a) Mahatma(R) Saffron YELLOW seasonings & LONG GRAIN RICE Recalled by...
The Issue: Foreign Material (Metal) in pouched Rice Mixes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raindrop Near Vision Inlay Recalled by Revision Optics Inc Due to ReVision...
The Issue: ReVision Optics has updated the instructions for use (IFU) for the Raindrop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.