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. 2,918 recalls have been distributed to Florida in the last 12 months.
Showing 4901–4920 of 30,686 recalls
Recalled Item: GORE VIABIL Short Wire Biliary Endoprosthesis Recalled by W.L. Gore &...
The Issue: Devices without transmural drainage holes may be mislabeled as devices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec Natura Stomahesive Post-Operative / Surgical Ostomy System Recalled...
The Issue: The kit contains a flange that has a 45mm coupling ring, however, the pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC*...
The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC* Gastric-Jejunal Feeding Tube Recalled by Avanos Medical, Inc. Due to...
The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: W&H Surgical handpiece S-12. For Surgical treatment of dental hard Recalled...
The Issue: 1:2 speed increasing surgical handpieces have been incorrectly laser marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The Emergency...
The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The...
The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Water Filter MAJ-2318. This MAJ-2318 water filter has been designed Recalled...
The Issue: Water filter may have been assembled incorrectly, resulting in unfiltered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...
The Issue: The kits contain saline flush syringes which were recalled by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...
The Issue: European version of microcatheter were distributed within US which contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...
The Issue: European version of microcatheter were distributed within US which contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.