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.
Showing 27941–27960 of 28,748 recalls
Recalled Item: MicroCool Breathable Gown with Towels Recalled by Kimberly-Clark Corporation...
The Issue: Package seam of some units may not remain properly sealed to ensure the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BP7561 OPTI CCA-TS B-Lac Cassette (25 per box) Cassettes are Recalled by...
The Issue: The values reported for PCO2 by BP7561 B-Lac cassettes are biased at high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is Recalled by...
The Issue: The IntraOs 70 system was found to have missing or incomplete system labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith &...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545...
The Issue: Three complaints have been filed where the Hoffman LRF Telescopic Struts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white...
The Issue: Distal part of the anchor may break on insertion into bone during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verify¿ Bowie-Dick Test Card Recalled by Steris Corporation Due to STERIS...
The Issue: STERIS has learned that the Verify Bowie Dick Test Cards are not performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Varian ARIA Oncology Information System Recalled by Varian...
The Issue: A software anomaly has been identified with the Import Export Application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY LIQUIBEADS Vaginal Moisturizer Recalled by Mc-NEIL-PPC, Inc. Due to...
The Issue: Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix...
The Issue: Ethicon and Omrix Biopharmaceuticals have received reports of air or gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL 9NC Coagulation Sodium Citrate 3.2% Recalled by Greiner Bio-One North...
The Issue: Part of the lot received a lower concentration of citrate solution which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bella Blanket Protective Coverlet Recalled by Beekley Corporation Due to...
The Issue: Imaging artifact can occur on mammogram result
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc....
The Issue: A routine internal quality check found that the Drager PT 4000 Phototherapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: Philips Healthcare was notified that several of the sixteen bolts securing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPIDER Surgical Instrument: Flexible Clip Applier The SPIDER¿ Surgical...
The Issue: Some clip applier units may be inadequate to achieve clip closure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge HEMO software. Recalled by Merge Healthcare, Inc. Due to The...
The Issue: The International Normalized Ratio (INR) value displayed in the study report...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chorus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sara Plus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due...
The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.