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. 2,710 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,710 in last 12 months

Showing 3014130160 of 55,837 recalls

Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: PRCT MIS CR MOB PLT SZ 4 L¿ PRCT MIS Recalled by Zimmer Biomet, Inc. Due to...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 10 INCH BEADED FC REV 15.0X250MM BWD LT & Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX OPT FEM C-R MINUS CR-FLEX OPT FEM D-L MINUS Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Smiths Medical ASD Inc.

Recalled Item: BCI Advisor Vital Signs Monitor Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Some printing modes on the devices may not function properly (tabular data...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2017· Alere San Diego Inc. DBA Immunalysis Corporation

Recalled Item: lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls Recalled by...

The Issue: The High (125 ng/ml) Control does not meet specification - it has been...

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

Class III — Low RiskOngoing
DrugNovember 28, 2017· EAI-JR286 INC

Recalled Item: Vertra Elemental Resistance (Octyl Methoxycinnamate 6% Recalled by EAI-JR286...

The Issue: CGMP Deviations: products manufactured in a manner that may impact product...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 28, 2017· Teva Pharmaceuticals USA

Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: high out of specification test...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 27, 2017· Cincinnati Sub-Zero Products LLC

Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...

The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Quad- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard BLUE PLUS Pressure Injectable Quad- Lumen CVC Kit Product...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ Large-Bore Multi-Lumen CVC Kit Product Usage: The Arrow¿...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...

The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Product Usage: The Arrow¿ CVC is indicated to Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R)...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit Product Usage:...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Arrow International Inc

Recalled Item: AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Recalled by...

The Issue: Some of the products listed in the recall may be missing a sticker that...

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

Class II — Potential Health HazardOngoing