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. 2,754 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,754 in last 12 months

Showing 2164121660 of 55,837 recalls

Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Medela Inc

Recalled Item: Invia Foam Dressing Kit with FitPad - X-Large (3 pcs) Recalled by Medela Inc...

The Issue: Invia Foam Dressing Kit with FitPad could have holes in the sterile packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Medical Action Industries, Inc. 306

Recalled Item: Medical convenience trays and kits Recalled by Medical Action Industries,...

The Issue: The kits contain a bottle of saline solution which may exceed the USP...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· 3-D Matrix, Inc.

Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...

The Issue: The boxes used by the shipper were not validated for use during transport.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Argon Medical Devices, Inc

Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...

The Issue: Incorrect product labeling.

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2019· AuroMedics Pharma LLC

Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugDecember 2, 2019· Preferred Pharmaceuticals, Inc

Recalled Item: Ranitidine Tablets Recalled by Preferred Pharmaceuticals, Inc Due to CGMP...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 2, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Amantadine Hydrochloride Tablets Recalled by Jubilant Cadista...

The Issue: Presence of Foreign Substance: Presence of a foreign object in a single tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2019· Pfizer Inc.

Recalled Item: 25% Dextrose Injection Recalled by Pfizer Inc. Due to Labeling: Incorrect or...

The Issue: Labeling: Incorrect or Missing Lot and/or expiration date.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula Recalled by Edwards Lifesciences, LLC Due to If the...

The Issue: If the venous cannula is used in an unintended manner (longer than 6 hours;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2019· Flexicare Medical Ltd.

Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...

The Issue: The firm has received reports that the spring/washer/bearing components in...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2019· SCA Pharmaceuticals, LLC

Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals, LLC Due to Foreign...

The Issue: Presence of Foreign Substance: Foreign material found inside the vial...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 26, 2019· Fuji Food Products, Inc.

Recalled Item: Trader Joe's 8pcs Spicy California Roll Recalled by Fuji Food Products, Inc....

The Issue: RTE products potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 26, 2019· Fuji Food Products, Inc.

Recalled Item: Trader Joe's 10oz Banh Mi Style Salad w/ Tofu Recalled by Fuji Food...

The Issue: RTE products potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 26, 2019· Fuji Food Products, Inc.

Recalled Item: Trader Joe's 8pcs Regular California Roll Recalled by Fuji Food Products,...

The Issue: RTE products potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 26, 2019· Fuji Food Products, Inc.

Recalled Item: Trader Joe's 8pcs Smoked Salmon Philly Roll Recalled by Fuji Food Products,...

The Issue: RTE products potentially contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund