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. 2,723 recalls have been distributed to Florida in the last 12 months.
Showing 25061–25080 of 55,837 recalls
Recalled Item: Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat...
The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for loss of the x-ray imaging function when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cleocin Phosphate (clindamycin injection) Recalled by Pfizer Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15 Recalled...
The Issue: Defective container: Ineffective seal between the cap and jar of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Randox Laboratories Ltd. Catalogue Number CQ5052 Recalled by Response...
The Issue: The form received three complaints related to the user obtaining a result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan 50mg Tablet Recalled by RemedyRepack Inc. Due to CGMP Deviations;...
The Issue: CGMP Deviations; Detection of trace amounts of an unexpected impurity found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blue Fusion Capsules Recalled by Ata International Inc Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Implant Retrieval Instrument CC RP & Tri Ch Hex WP Recalled by Nobel Biocare...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Instrument CC NP & Ext Hex WP 22 Recalled by Nobel Biocare...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Screw Tap Tapered WP Single-Pat - Product Usage: The Guided Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered WP 5x10 mm Single-Pat - Product Usage: Drills Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: Recalled by Nobel...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Recalled by Nobel...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Retrieval Instrument Hex & Tri-Ch NP/RP 22mm - Product Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Tapered 6.0 6x8 mm Single-Pat - Product Usage: Drills Recalled by...
The Issue: Due to a problem in the packaging sealing process at the supplier of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.