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. 1,729 recalls have been distributed to Kentucky in the last 12 months.
Showing 43901–43920 of 51,386 recalls
Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...
The Issue: Defective Delivery System; defective valve
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
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.
Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Nylon fibers found in a bottle of 0.9%...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Confirmed customer complaint that orange and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Orally Disintegrating Tablets 5 mg Recalled by Apotex Corp. Due...
The Issue: Subpotent Drug: Out of specification (OOS) results at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.