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. 989 recalls have been distributed to Kentucky in the last 12 months.
Showing 33841–33860 of 51,386 recalls
Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 28CM Item Code: E278228 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Linear Accelerator Recalled by Elekta, Inc. Due to There have been...
The Issue: There have been instances in hospitals where the joint between the drive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode Retractable 28CM Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes Item Code:...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277336 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode 45CM Item Code: E277145 The...
The Issue: Potential for compromise of the package resulting in a breach of the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...
The Issue: Arrow is recalling due to incorrect labeling of products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego Recalled by Siemens Medical Solutions USA, Inc Due to Due...
The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...
The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Krusteaz Blueberry Pancake Mix Recalled by Continental Mills (Corporate...
The Issue: Krusteaz Blueberry Pancake Mix is recalled due to a potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk packaged flour based tortilla bits packaged in 45.5 lb. bags. Recalled...
The Issue: The supplier received flour from General Mills that was contaminated with E....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk packaged flour based "breader" packaged in 25 Recalled by Newly Weds...
The Issue: The supplier received flour from General Mills that was contaminated with E....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...
The Issue: This field action is being initiated following the firm's discovery of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COCONUT SHRIMP Recalled by Kabobs Inc Due to Potential E. coli Contamination
The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINI VEGETABLE EGGROLL Recalled by Kabobs Inc Due to Potential E. coli...
The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.