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.
Showing 27101–27120 of 30,686 recalls
Recalled Item: Synergy XVI The Elekta Synergy S is intended to be Recalled by Elekta, Inc....
The Issue: Potential collision risk when using XVI and external beam shaping devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Abbott m2000sp is an automated system for performing sample Recalled by...
The Issue: The x-drive assembly may fail prematurely. This could cause the manipulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...
The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
Recalled Item: G1762: 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.
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.
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.
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.
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.
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.
Recalled Item: 3M ESPE Imprint II Regular Body Recalled by 3M Company - Health Care...
The Issue: Specific lots of Imprint II and Paradigm impression material packs are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normative Data Template CD for use with the I-Portal devices. Used to...
The Issue: The data provided on the Normative Data Template CD for use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.