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. 2,698 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,698 in last 12 months

Showing 3332133340 of 55,837 recalls

DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: BIGnHARD Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: ZRECT for Women Herbal Dietary Supplement Capsules Recalled by Organic...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: TORNADO Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: ZRECT Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: UPROAR All Natural Male Enhancement Herbal Dietary Supplement Capsules...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: LabidaMAX Herbal Dietary Supplement Capsules Recalled by Organic Herbal...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: RECTALIS Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: Cummor Natural Male Enhancement Recalled by Organic Herbal Supply Due to...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: ENHANCEROL Herbal Dietary Supplement Capsules Recalled by Organic Herbal...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: Xrect Male Enhancement Herbal Dietary Supplement Capsules Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Organic Herbal Supply

Recalled Item: ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement...

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the presence of...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 18, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Riomet (metformin hydrochloride) Oral Solution Cherry Flavored 500 mg /5 mL...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2017· Abbott Laboratories

Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...

The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2017· Zimmer Biomet, Inc.

Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...

The Issue: nail not properly engaging with the targeting jig due to certain undersized...

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

Class II — Potential Health HazardOngoing
FoodApril 17, 2017· Moondance Heavenly Desserts, LLC

Recalled Item: Moondance desserts gluten free Mexican Wedding Cookie 8 oz (227g) Recalled...

The Issue: undeclared pecans

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

Class III — Low RiskOngoing
Refund
FoodApril 17, 2017· Moondance Heavenly Desserts, LLC

Recalled Item: Moondance desserts gluten free Chocolate Chip Cookie Bar 12 oz Recalled by...

The Issue: undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2017· P & L Development, LLC

Recalled Item: Allergy Relief Diphenhydramine HCl 25 mg Recalled by P & L Development, LLC...

The Issue: Subpotent: This product is being recalled due to low out of specification...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2017· Fagron, Inc

Recalled Item: Zinc Oxide Paste 25% Recalled by Fagron, Inc Due to Labeling: Error on...

The Issue: Labeling: Error on Declared Strength: Error is due to an incorrect value in...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 14, 2017· Cardiovascular Systems Inc

Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...

The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2017· Del Mar Reynolds Medical, Ltd.

Recalled Item: Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use...

The Issue: Reports of the Canister Carrier breaking during absorbent exchange or during...

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

Class II — Potential Health HazardOngoing