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. 1,894 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,894 in last 12 months

Showing 4076140780 of 55,837 recalls

DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Extreme Stack Fat Burner Dietary Supplement packaged Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Naturally The Natural Alternative AM Dietary Supplement...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Fataway Ultimate Stack with Chromium Recalled by Novacare, LLC...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim MaxOut Body Max Out FX Fat Burner Recalled by Novacare, LLC...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant Recalled...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: P.M. (Mineral Oil 42.5% and White Petrolatum 57.3%) Lubricant Recalled by...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· C. O. Truxton

Recalled Item: Doxycycline Hyclate Tablets Recalled by C. O. Truxton Due to Labeling: Wrong...

The Issue: Labeling: Wrong Bar Code

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: FML (fluorometholone ophthalmic ointment) 0.1% Recalled by Allergan Sales,...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Solution...

The Issue: Lack of Assurance of Sterility; potential exposure to non-sterile lubricant...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Silarx Pharmaceutical, Inc.

Recalled Item: Lamivudine Oral Solution Recalled by Silarx Pharmaceutical, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a...

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

Class III — Low RiskOngoing
Refund
DrugAugust 21, 2015· Akorn, Inc.

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn, Inc. Due to...

The Issue: Defective Container: Product missing safety seal around the neck of the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 21, 2015· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 Recalled by Olympus...

The Issue: Insufficient information for specific cleaning accessories used for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2015· DJO, LLC

Recalled Item: Monode Recalled by DJO, LLC Due to Overheating and burning of the wire...

The Issue: Overheating and burning of the wire insulation inside the applicator.

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

Class II — Potential Health HazardOngoing
DrugAugust 21, 2015· Nephron Pharmaceuticals Corp.

Recalled Item: Asthmanefrin Racepinephrine Inhalation Solution Bronchodilator...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection Recalled by Cantrell...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: MIDAZOLAM HCl in 0.9% Sodium Chloride Injection Recalled by Cantrell Drug...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection Recalled by...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2015· Cantrell Drug Company

Recalled Item: HEPARIN Sodium in 0.45% Sodium Chloride Recalled by Cantrell Drug Company...

The Issue: Stability Data Does Not Support Expiry

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

Class II — Potential Health HazardOngoing
Refund