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. 2,923 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,923 in last 12 months

Showing 41214140 of 13,925 recalls

DrugApril 13, 2021· Nomax Inc

Recalled Item: Dry Eye Test Recalled by Nomax Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugApril 12, 2021· Edge Pharma, LLC

Recalled Item: Betadine (Povidone-Iodine) 5% Recalled by Edge Pharma, LLC Due to Defective...

The Issue: Defective container; syringe content migrating past the seal of the plunger...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 9, 2021· Teligent Pharma, Inc.

Recalled Item: Flurandrenolide Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2021· NSNY Distributor Inc

Recalled Item: Ginseng Power 5000 capsule Recalled by NSNY Distributor Inc Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 8, 2021· NSNY Distributor Inc

Recalled Item: Premium OrgaZEN 7000 capsule Recalled by NSNY Distributor Inc Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Black 5000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: Triple SupremeZen Plus 3500 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2021· Hyobin LLC

Recalled Item: PremierZen Extreme 3000 Recalled by Hyobin LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 1, 2021· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Itraconazole Capsules Recalled by Jubilant Cadista Pharmaceuticals, Inc. Due...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Imperial Platinum 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Burro en Primavera Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: IMPERIAL GOLD 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· Apotex Corp.

Recalled Item: Guanfacine Extended-Release Tablets 2 mg Recalled by Apotex Corp. Due to...

The Issue: Cross Contamination with Other Product: Product is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Thumbs up 7 Red 70K capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Shogun-X capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Krazy Night capsule Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Na Na Collection

Recalled Item: Triple SupremeZen Gold 3500 Recalled by Na Na Collection Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2021· Na Na Collection

Recalled Item: PremierZen Platinum 5000 Recalled by Na Na Collection Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund