Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,457 in last 12 months

Showing 2474124760 of 28,748 recalls

Medical DeviceApril 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: Recalled by...

The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2014· Medtronic Navigation, Inc.

Recalled Item: ENT PRGM 9734636 ADD FUSION NAV AxiEM Recalled by Medtronic Navigation, Inc....

The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· C P Medical Inc.

Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...

The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· CareFusion 303, Inc.

Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...

The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 23, 2014· Heraeus Kulzer, LLC.

Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...

The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...

The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2014· Smiths Medical ASD, Inc.

Recalled Item: SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket Recalled by...

The Issue: The hose could separate from the blanket.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2014· Biomet, Inc.

Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...

The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2014· Hamilton Medical, Inc.

Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....

The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 21, 2014· Aesculap, Inc.

Recalled Item: Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt...

The Issue: AIC (USA) received information regarding 3 complaints in which the deflector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2014· Bausch & Lomb Inc- Greenville Solutions Plant

Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...

The Issue: Out of specification results for one of the two disinfectants.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Leica Microsystems, Inc.

Recalled Item: Thyroglobulin (1D4) is a mouse anti-human monoclonal antibody produced as...

The Issue: Bond Ready to Use Primary Antibody Thyroglobulin does not function as...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Elekta, Inc.

Recalled Item: HexaPOD evo RT Couchtop. To support and aid in positioning Recalled by...

The Issue: If screws are not properly tightened with a torque wrench they may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Gen-Probe Inc

Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...

The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2014· Mckesson Medical Immaging

Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...

The Issue: High priority alert icon was not displayed in the Study List when there are...

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

Class II — Potential Health HazardOngoing