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 3998140000 of 55,837 recalls

Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 3F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Over-the-Wire Embolectomy Catheter 7F Recalled by LeMaitre...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2015· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 5F Recalled by LeMaitre Vascular,...

The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2015· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: Presence of Foreign Tablets/Capsules: one foreign capsule identified as...

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

Class III — Low RiskOngoing
Refund
DrugOctober 21, 2015· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION Recalled by Vintage...

The Issue: Failed Stability Specifications: Out of Specification results obtained for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart 11 Test Cup Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 11 Panel Dip Card (OPI 2000) Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 12-Panel Dip Drug Screen with adulterant Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: Micro Screen 6 Panel Cup with Adult (AU) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: ArcPoint Labs 10 Panel Dip Screen (OXY) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 11 Panel Cup (OPI2000) w/Adult Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: EDI BZO UNCUT SHEET-CARD Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart 10 Test Cup (PCP & MDMA) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: ProScreen 10 Drug Panel Cassette Test Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU) Recalled by...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: Premier Clia Waived 12 panel Tilt Cup Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugCheck Pipette 10 Drug Test Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 1 Step 12 Panel Cup Recalled by Ameditech Inc Due to Ameditech is recalling...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing