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 3302133040 of 55,837 recalls

Medical DeviceApril 21, 2017· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain Recalled by Cardinal Health 200,...

The Issue: Product's seal possibly compromised, potentially compromising the sterility...

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

Class II — Potential Health HazardOngoing
FoodApril 21, 2017· Frito-Lay, Inc

Recalled Item: 30 count Miss Vickies Multipack Tray 41.25 oz. packaged in flexible plastic...

The Issue: Potential presence of Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2017· Frito-Lay, Inc

Recalled Item: 20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexible plastic...

The Issue: Potential presence of Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2017· Frito-Lay, Inc

Recalled Item: Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape¿o Flavored...

The Issue: Potential presence of Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2017· Frito-Lay, Inc

Recalled Item: 30 count Lays Kettle Cooked Multipack Tray 41.25 oz. packaged Recalled by...

The Issue: Potential presence of Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2017· Frito-Lay, Inc

Recalled Item: 12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged in flexible...

The Issue: Potential presence of Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2017· Frito-Lay, Inc

Recalled Item: 32 count Miss Vickies Multipack Box 44 oz. packaged in flexible plastic...

The Issue: Potential presence of Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 20, 2017· Global Lam Sheng Kee inc.

Recalled Item: Lam Sheng Kee Frozen Fried Tofu NET Weight 240g(8.5 OZ) Recalled by Global...

The Issue: Product may contain undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 20, 2017· Global Lam Sheng Kee inc.

Recalled Item: Lam Sheng Kee Frozen White Fish Ball NET WEIGHT: 32.1 OZ Recalled by Global...

The Issue: Product may contain undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 20, 2017· Global Lam Sheng Kee inc.

Recalled Item: Lam Sheng Kee Frozen Fried Fish Ball NET WEIGHT: 227g (8oz) Recalled by...

The Issue: Product may contain undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Labeling: Labeled...

The Issue: Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· C. O. Truxton

Recalled Item: Amitriptyline HCL Tablets Recalled by C. O. Truxton Due to Mislabeling

The Issue: Labeling: Label Mixup; potentially mislabeled

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2017· Akorn, Inc.

Recalled Item: IC-Green (indocyanine green for injection Recalled by Akorn, Inc. Due to...

The Issue: Product is being recalled due to low pH value.

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 20, 2017· Biomerieux Inc

Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N293) Recalled by Biomerieux...

The Issue: The integrity of the product container may be compromised thereby exposing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· Vortran Medical Technology 1, Inc

Recalled Item: VORTRAN Automatic Resuscitator Recalled by Vortran Medical Technology 1, Inc...

The Issue: Vortran received a customer complaint that the spin-nut-DSS connector was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2017· EBI Patient Care, Inc.

Recalled Item: 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a Recalled...

The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...

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

Class I — Serious Health HazardOngoing