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. 2,939 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,939 in last 12 months

Showing 20212040 of 13,925 recalls

DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Midazolam Injection Recalled by Akorn, Inc. Due to CGMP Deviations: Firm...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Calcipotriene Topical Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Apotex Corp.

Recalled Item: Calcitonin Salmon (synthetic origin) Nasal Spray Recalled by Apotex Corp....

The Issue: Presence of Foreign Substance: Glass splinter particle entrapped inside the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Gadget Island, Inc

Recalled Item: DYNAMITE SUPER capsule Recalled by Gadget Island, Inc Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 26, 2023· Gadget Island, Inc

Recalled Item: Pro Power Knight Plus capsule Recalled by Gadget Island, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 26, 2023· Gadget Island, Inc

Recalled Item: NUX Male Enhancement capsule Recalled by Gadget Island, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 24, 2023· The Harvard Drug Group

Recalled Item: Gabapentin Tablets Recalled by The Harvard Drug Group Due to Product mixup:...

The Issue: Product mixup: one foreign tablet found in product.

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2023· Bryant Ranch Prepack, Inc.

Recalled Item: Lidocaine Patch 5% Recalled by Bryant Ranch Prepack, Inc. Due to Labeling:...

The Issue: Labeling: Typographical error on the upper left-hand side of the box and...

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

Class III — Low RiskOngoing
Refund
DrugApril 19, 2023· Seatex LLC

Recalled Item: Seatex Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile...

The Issue: Superpotent Drug and Failed Impurities/Degradation Products: formula does...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2023· Sun Pharmaceutical Industries Ltd.

Recalled Item: Fyremadel (ganirelix acetate) injection Recalled by Sun Pharmaceutical...

The Issue: Presence of Particulate Matter: A piece of glass was found in a prefilled...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-200 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel DG Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-102 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-101 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 11, 2023· Sanofi-Aventis U.S. LLC

Recalled Item: Admelog Recalled by Sanofi-Aventis U.S. LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Malformed crimped collar seal

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2023· SCA Pharmaceuticals

Recalled Item: Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL Recalled by SCA...

The Issue: Subpotent Drug: Out of specification results for low potency was obtained.

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

Class III — Low RiskOngoing
Refund
DrugApril 7, 2023· Methapharm Inc

Recalled Item: Pantoprazole sodium for Injection 40 mg*/vial Recalled by Methapharm Inc Due...

The Issue: CGMP Deviations; The impacted product and lot number was inadvertently...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Simvastatin USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP deviations.

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2023· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Glimepiride USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP deviations.

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund