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. 2,739 recalls have been distributed to Florida in the last 12 months.
Showing 22481–22500 of 55,837 recalls
Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...
The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mero Macho Artificially Flavored Passion Fruit Vitamin C Liquid Supplement...
The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gold Medal Enriched Recalled by General Mills, Inc Due to Potential E. coli...
The Issue: 5 lb. bags of Gold Medal Unbleached All Purpose flour have the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IceCure Cryoablation System ProSense -Intended for cryogenic destruction of...
The Issue: Updated User Manual DSR3200000 Rev. E to include the safety guidelines in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...
The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...
The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...
The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: There is a potential performance issue as detected by an under-recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: There is a potential performance issue as detected by an under-recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: There is a potential performance issue as detected by an under-recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...
The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...
The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...
The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI:...
The Issue: A portion of the lot was incorrectly packaged with a 12.5cm catheter instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...
The Issue: Potential for failure of the patient leakage current test. There is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Injection USP 0.9% Recalled by GUERBET LLC Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Optiray 320 (ioversol) Injection 68% Recalled by GUERBET LLC Due to...
The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abbott Calcilo XD Recalled by Abbott Laboratories Due to Off color and odor....
The Issue: Off color and odor. Compromised can seam due to product (powder) in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Infinity Acute Care System (IACS) Monitoring Solution with the Recalled...
The Issue: Cybersecurity vulnerabilities may cause device to reboot, lose alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sermorelin Recalled by KRS Global Biotechnology, Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.