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. 1,075 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,075 in last 12 months

Showing 19201–19220 of 55,837 recalls

Medical DeviceAugust 31, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK TIN ABUTMENT 4.1MM Number: IEDAN4 Recalled by Biomet 3i,...

The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK TIN ABUTMENT 5.0MM Number: IEDAN5 Recalled by Biomet 3i,...

The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· Biomet 3i, LLC

Recalled Item: CERTAIN BELLATEK TITANIUM ABUTMENT 4.1MM Number: IEDAT4 Recalled by Biomet...

The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2020· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Potential for...

The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2020· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator Recalled by Greiner...

The Issue: Blood collection tubes experienced an issue with separation and clotting

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2020· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens epoc BGEM Test Card-In vitro diagnostic device for the Recalled by...

The Issue: Sporadically inconsistent discrepant (low bias) glucose results on card lot...

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

Class II — Potential Health HazardOngoing
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Whole Foods Market Organic White Cheddar Popcorn Recalled by EAGLE...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Nature's Promise Organic Lightly Salted Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· Preferred Popcorn

Recalled Item: Organic Yellow Popcorn packaged in the following ways: 1) Great Recalled by...

The Issue: Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Nice! Organic White Cheddar Popcorn Recalled by EAGLE FAMILY FOODS GROUP LLC...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn Recalled by EAGLE...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: Cretors Organic Extra Virgin Olive Oil Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 28, 2020· EAGLE FAMILY FOODS GROUP LLC

Recalled Item: 365 Everyday Value Organic Classic Salted Popcorn Recalled by EAGLE FAMILY...

The Issue: Foreign material, pieces of glass may be in the product

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 27, 2020· Treehouse Foods

Recalled Item: Signature Select Chewy Granola Bars Recalled by Treehouse Foods Due to...

The Issue: Product may contain undeclared peanut butter.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 27, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Albumin Gen.2 Recalled by Roche Diagnostics Operations, Inc. Due to Roche...

The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...

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

Class III — Low RiskOngoing
Medical DeviceAugust 27, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-quant Complement C4 ver.2 Recalled by Roche Diagnostics Operations,...

The Issue: Roche has confirmed customer complaints of low quality (QC) recovery and...

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

Class III — Low RiskOngoing
Medical DeviceAugust 26, 2020· ev3 Inc.

Recalled Item: Pacific Xtreme (PTCA Balloon Dilation Catheter) Recalled by ev3 Inc. Due to...

The Issue: Labeling discrepancy for the Rated Burst Pressure (RBP) value.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2020· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol...

The Issue: Due to alkaline phosphatase (ALP) associated interference causing falsely...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2020· Wright Medical Technology Inc

Recalled Item: EVOLVE STEM 8.5MM Model # 496S085 Recalled by Wright Medical Technology Inc...

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardOngoing