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. 2,670 recalls have been distributed to Florida in the last 12 months.
Showing 38221–38240 of 55,837 recalls
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Calretinin Recalled by Leica...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Calretinin when used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...
The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics GBS Detect Cat no. A300. Used for the Recalled by Hardy...
The Issue: Performance failure; poor hemolytic reaction of non or weakly hemolytic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver...
The Issue: Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD-Retic-Count Reticulocyte Reagent System Recalled by Becton, Dickinson and...
The Issue: The carton label for one lot of BD Retic-Count Reticulocyte Reagent System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as an insect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elderberry 500 mg packaged in a white and orange bottle Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Andrographis extract 400 mg packaged in a white and orange Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cranberry extract packaged in a white and orange bottle containing Recalled...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Goldenseal Root 500 mg packaged in a white and orange Recalled by NOW Foods...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.