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. 2,670 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,670 in last 12 months

Showing 3806138080 of 55,837 recalls

Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Reamer....

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Recalled by B...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
FoodApril 1, 2016· Platinum Distribution Inc

Recalled Item: R No Sugar Added Recalled by Platinum Distribution Inc Due to Manufacturer...

The Issue: Manufacturer Ross Chocolates, Coquitlam, BC Canada recalled these chocolate...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2016· Roland Foods, LLC.

Recalled Item: Roland (R) Fire Roasted Red Pepper Strips Recalled by Roland Foods, LLC. Due...

The Issue: Possible presence of glass fragments in the product lots.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 1, 2016· Sugarfina, LLC

Recalled Item: Sugarfina Chocolate Malt Balls Code 840278113565 SKU K1159 Recalled by...

The Issue: undeclared peanuts

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 31, 2016· International Sprout Holding Inc.

Recalled Item: ALFALFA SEED Recalled by International Sprout Holding Inc. Due to Potential...

The Issue: One sample taken were positive for Salmonella Poly B

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 31, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...

The Issue: E. CAM and Symbia system with foresight detectors performing gated or...

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

Class II — Potential Health HazardOngoing
DrugMarch 31, 2016· Amerisource Health Services

Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 31, 2016· Invisiblu International LLC

Recalled Item: LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due...

The Issue: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2016· Amerisource Health Services

Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 31, 2016· Purdue Pharma L.P.

Recalled Item: Intermezzo (zolpidem tartrate) sublingual tablet 1.75 mg Recalled by Purdue...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 13 mm x 60 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1.5" : 20-06S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 3/4" : 30-03 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Policot 1/2" x 1/2" : 90-06 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 15 mm x 15 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 3" : 60-09 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 70 mm x 10090 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing