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. 2,555 recalls have been distributed to Kentucky in the last 12 months.
Showing 16721–16740 of 28,748 recalls
Recalled Item: 7" Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Smallbore Ext Set w/MicroClave¿ Recalled by ICU Medical, Inc. Due to The...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx. 0.57 ml Recalled by ICU Medical, Inc. Due to The infusion...
The Issue: The infusion sets were manufactured with an incorrect spin collar.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans FILTRON 250 Recalled by Shippert Medical Technologies Due to The...
The Issue: The pouch integrity of the sterile product can't be assured without a visual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Surgical Clipper Professional 9681 Recalled by 3M Company - Health Care...
The Issue: Failure to follow proper charging practices can result in lithium-ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature...
The Issue: This recall has been identified due to the batch being mislabeled, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...
The Issue: Supplier manufacturing defect with the syringe plunger tip.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to Recalled by Dako...
The Issue: To correct the kit's instructions for use as the storage time for gastric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope Power (Model 10967888) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline 0.9 % Sodium Chloride Injection Recalled by Medline Industries Inc...
The Issue: Packaged with an incorrect overwrap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 (Model 10165888) Recalled by Siemens Medical Solutions...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Scope ( Model 10967666) Recalled by Siemens Medical Solutions USA,...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 (10165977) Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A potential risk of unnecessary radiation exposure due to a software issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.