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. 935 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
935 in last 12 months

Showing 48781–48800 of 55,837 recalls

Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1725: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...

The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1469J: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4040-2: Umbilical 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043W-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043G-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G2001: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: G1777: Umbilical (2) 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042LH: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

Recalled Item: 4042E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...

The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System....

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Medrad Mr Inc

Recalled Item: Medrad Veris MR Monitor units The system is intended to Recalled by Medrad...

The Issue: The main board, P/N 301641, installed in some Medrad Veris MR Monitor units...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA N Control Recalled by Horiba Instruments, Inc dba Horiba Medical...

The Issue: Horiba Medical is recalling the ABX PENTRA N Control because it has been...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Steris Corporation

Recalled Item: SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled by Steris...

The Issue: Customers indicated fluctuations in environmental conditions sites and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Ziehm Imaging Inc

Recalled Item: Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile...

The Issue: Engineering change in 2006 resulted in a minor non-conformity of their...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2013· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Testing Disc Recalled by Remel Inc Due to...

The Issue: Individual discs in the lot may not be sufficiently impregnated with...

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

Class II — Potential Health HazardOngoing