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. 2,801 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,801 in last 12 months

Showing 1890118920 of 55,837 recalls

DrugOctober 8, 2020· Denton Pharma, Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP 750 mg Recalled by...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 8, 2020· Enterix, Inc.

Recalled Item: InSure ONE Test Strips (25 pack) vials-fecal immunochemical test (FIT)...

The Issue: Product does not meet internal testing criterion; use of the product may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2020· Canon Medical System, USA, INC.

Recalled Item: CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Recalled by...

The Issue: There is a potential that the cable of the Flat panel detector may break...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation standalone software treatment planning system Recalled by...

The Issue: If a region of interest (ROI) or point of interest (POI) that is from an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2020· Microbiologics Inc

Recalled Item: Catalog 02145P Recalled by Microbiologics Inc Due to Strain should be VIM-1...

The Issue: Strain should be VIM-1 positive but is confirmed to be VIM-1 negative.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 7, 2020· Baxter Healthcare Corporation

Recalled Item: Bupivacaine Hydrochloride in 8.25% Dextrose Injection Recalled by Baxter...

The Issue: Presence of particulate matter in solution - black and transparent particles

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2020· Steris Corporation

Recalled Item: Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning...

The Issue: Potential for cleaning solution intrusion into endoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
DrugOctober 6, 2020· PD-Rx Pharmaceuticals, Inc.

Recalled Item: metformin HCL ER 750 mg Rx only Pkg By: PD-Rx Recalled by PD-Rx...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2020· PD-Rx Pharmaceuticals, Inc.

Recalled Item: metformin HCL ER 500 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 6, 2020· Ariola Foods Corp.

Recalled Item: Frozen raw Lobster Tail pastry 100 count Recalled by Ariola Foods Corp. Due...

The Issue: Lobster tail pastry contains undeclared wheat, FD&C Red #40, and FD&C Yellow...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2020· Arjohuntleigh Magog, Inc.

Recalled Item: Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used Recalled by...

The Issue: Risk of Sling Clip breakage while in use with obsolete Flat Dynamic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2020· Exactech, Inc.

Recalled Item: Catalog 314-13-23 Recalled by Exactech, Inc. Due to Mislabeling

The Issue: The product may be mislabeled.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2020· Exactech, Inc.

Recalled Item: Catalog 314-13-33 Recalled by Exactech, Inc. Due to Mislabeling

The Issue: The product may be mislabeled.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2020· Hardy Diagnostics

Recalled Item: Strep B Carrot Broth One-Step Recalled by Hardy Diagnostics Due to...

The Issue: Streptococcus culture medium contains an incorrect expiration date. The...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2020· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Catapres (clonidine hydrochloride Recalled by Boehringer Ingelheim...

The Issue: An extraneous peak was observed for dissolution testing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgG Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: The cross-reactivity of the device may present an increased level of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Recalled by Becton,...

The Issue: Recent product complaints showing an unexpected cell population exhibiting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Bayer Medical Care, Inc.

Recalled Item: Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic...

The Issue: Specific lots of MEDRAD Stellant FLEX 150 mL syringe kits may have holes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing