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. 2,754 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,754 in last 12 months

Showing 2150121520 of 55,837 recalls

Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 23G VFI Cannula-.D03 GTIN: 8719214221423 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G VFI Cannula-.D03 GTIN: 8719214221447 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Silicone Tipped Cannula-.D01 GTIN: 8719214221522 Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 20G VFI Cannula-.D03 GTIN: 8719214221485 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Arthrex, Inc.

Recalled Item: Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile...

The Issue: There is a potential for blockage of the Hub Attachment Tube.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 23G PFC Injection Needle- .D01 GTIN: 8719214221362 Recalled by Vitreq...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 23G Silicone Tipped Cannula-CN23.D01 GTIN: 8719214221508 Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G PFC Injection Needle-.D01 GTIN: 8719214221386 Recalled by Vitreq...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Pick Needles-.D04 GTIN: 8719214221607 Recalled by Vitreq Bv Due...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Blunt Needles with luer-lock connector-.D05 GTIN: Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G VFI Cannula-.D03 GTIN: 8719214221461 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1) VitreQ 20G BF Blunt Needles-.D51 GTIN: 8719214221089 (2) Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G Blunt Needles with luer-lock connector-.D05 GTIN:8719214221669...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
DrugDecember 16, 2019· Akorn Inc

Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...

The Issue: Subpotent Drug: Low Out of specification (OOS) assay results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugDecember 16, 2019· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodDecember 16, 2019· MUNK PACK INC

Recalled Item: Munk Pack Peanut Butter Dark Chocolate Nut & Seed Bar Recalled by MUNK PACK...

The Issue: Product may contain undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 16, 2019· MUNK PACK INC

Recalled Item: Munk Pack Keto Nut and Seed Dark Chocolate Sea Salt Bar Recalled by MUNK...

The Issue: Product may contain undeclared milk

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

Class II — Potential Health HazardOngoing
Refund