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. 2,634 recalls have been distributed to Kentucky in the last 12 months.
Showing 7741–7760 of 51,386 recalls
Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...
The Issue: Due to an increased risk of degradation of the power entry switch resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCF-H190DL Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF-HQ190L EVIS EXERA III COLONOVIDEOSCOPE Recalled by Aizu Olympus Co., Ltd....
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...
The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCF-H190L Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIF-H190 Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may have...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIF-HQ190 Recalled by Aizu Olympus Co., Ltd. Due to Specific devices may...
The Issue: Specific devices may have an improperly repaired light guide connector due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was found in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: JayRobb Vanilla Flavored Egg White Protein Powder. Net Weight 24 Recalled by...
The Issue: foreign material - plastic
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits:...
The Issue: Produced with unintended open slits on the side of the mouthpiece body, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novum IQ Syringe infusion system Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...
The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-P190 Recalled by...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-i Recalled by Maquet Medical Systems USA Due to It was found that...
The Issue: It was found that the fixation (weld) employed by the supplier of the nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS Model Number BF-XT190 Recalled by...
The Issue: There is a risk of endobronchial combustion if high-frequency cauterization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.