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 2100121020 of 30,686 recalls

Medical DeviceSeptember 13, 2016· Tearscience, Inc

Recalled Item: LipiFlow thermal Pulsation System Recalled by Tearscience, Inc Due to...

The Issue: Complaints related to an error condition occurring during patient treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2016· TEM Systems Inc

Recalled Item: ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US...

The Issue: Customers complained of low/empty reagent vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Contour Fabricators Inc

Recalled Item: Zero-Gravity Radiation Protection System Radiology Personnel protective...

The Issue: Two customer complaints suggest that excessive rotation of the cable in one...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2016· Teleflex Medical

Recalled Item: Teleflex Percuaneous Solutions Recalled by Teleflex Medical Due to The...

The Issue: The product is being recalled due to a labeling error. The Gripper Graspers...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Ortho-Clinical Diagnostics

Recalled Item: enGen Laboratory Automation System (Product Code ENGEN) configured with...

The Issue: Ortho confirmed that it is possible for the mis-association of sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Celerity ECG Cable Accessory Pack Recalled by Angiodynamics Inc. (Navilyst...

The Issue: The Celerity ECG Cable Accessory Pack has the potential to contain an ECG...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2016· Ellman International, Inc.

Recalled Item: ellman A CYNOSURE COMPANY Minor Surgery Bipolar Cable Recalled by Ellman...

The Issue: Mislabeling of the "expiration date". The expiration date on the outer box...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software upgrade to eliminate several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2016· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the AQUIOS CL System because the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza VB10A Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Software upgrade to eliminate several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 405 Measurement Cartridge Siemens SMN numbers: 10844812...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 400 Measurement Cartridge Siemens SMN numbers:10329756...

The Issue: Error in the value assignment for the Chloride calibrators in the RAPIDPoint...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 2, 2016· Trilliant Surgical Ltd.

Recalled Item: Model 208-70-110 Recalled by Trilliant Surgical Ltd. Due to Screws were...

The Issue: Screws were identified as having the incorrect part number and lot number...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Arrow International Inc

Recalled Item: HANDS-OFF Infusion Port Thermodilution Catheter consists of the Arrow IPTD...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2016· Heritage Medical Products, Inc.

Recalled Item: 2000 Vascular with 30 Degree option Recalled by Heritage Medical Products,...

The Issue: Potential for bed to drop suddenly at the head while a patient is laying on it.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2016· Medtronic Navigation, Inc.

Recalled Item: Visualase Body Accessory Kit PN 020-3000. The individual components within...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2016· Medtronic Navigation, Inc.

Recalled Item: Visualase Visualization Stylets PN 020-2301. The individual components...

The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2016· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to RaySearch became...

The Issue: RaySearch became aware of the problem as it was discovered in cooperation...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2016· Ormco/Sybronendo

Recalled Item: Sealapex Xpress Recalled by Ormco/Sybronendo Due to SybronEndo is recalling...

The Issue: SybronEndo is recalling the Sealapex Xpress because it was labeled with an...

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

Class II — Potential Health HazardOngoing