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. 2,739 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,739 in last 12 months

Showing 2240122420 of 55,837 recalls

FoodSeptember 28, 2019· Adm Milling

Recalled Item: Robin Hood All-purpose Flour in 5 lb bag Recalled by Adm Milling Due to...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Best Baker's flour 50 lbs bags Recalled by Adm Milling Due to Potential E....

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: King Arthur All Purpose Flour 25# bags Recalled by Adm Milling Due to...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Bakers Corner All Purpose Flour in 5 lb. bags Recalled by Adm Milling Due to...

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Commander Flour Recalled by Adm Milling Due to Potential E. coli Contamination

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2019· Adm Milling

Recalled Item: Bulk flour Recalled by Adm Milling Due to Potential E. coli Contamination

The Issue: E.coli O26

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 27, 2019· Images Unlimited Products, dba Cellect Products

Recalled Item: CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered...

The Issue: Product contains unsafe levels of Arsenic and Lead

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Arbor Pharmaceuticals Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Arbor Pharmaceuticals Inc. Due...

The Issue: Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Alkermes, Inc.

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2019· Epic Pharma, LLC

Recalled Item: Estradiol tablets Recalled by Epic Pharma, LLC Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: Estradiol 1 mg was found in a 100...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 26, 2019· AMPLE HILLS MANUFACTURING

Recalled Item: Ample Hills Peppermint Pattie ice cream packed in 3 gallon Recalled by AMPLE...

The Issue: Product may contain undeclared peanut allergen

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 26, 2019· Life Technologies Holdings Pte Ltd

Recalled Item: Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 Recalled...

The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2019· Theralase Inc.

Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...

The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...

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

Class III — Low RiskOngoing