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. 1,890 recalls have been distributed to Kentucky in the last 12 months.
Showing 21301–21320 of 51,386 recalls
Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...
The Issue: Subpotent Drug: Out of specification result during stability study in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a...
The Issue: FungusAmongUs Shiitake Organic Mushrooms are recalled due to undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOMOD PORCOAT HA GLENTRAY Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALL NOSE GUIDE WIRE 80CM Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Hip systems Recalled by Zimmer Biomet, Inc. Due to Elevated levels...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HA Pins (DFS HA Cort Screw) Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive RS Cleat CAP Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Recalled by...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LT DISC ULNA - HA/PC Recalled by Zimmer Biomet, Inc. Due to Elevated levels...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENNESSY LEFT CONST GLENOID HA Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Products Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copeland HA Resurfacing Head Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0MM BALL NOSE GUIDE WIRE Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive HHR Tess Cleat Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GUIDE WIRE 2.2MM X 28IN Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioEnvelope Recalled by AZIYO BIOLOGICS Due to Possible suture brittleness...
The Issue: Possible suture brittleness or breakage along the Envelope seam before the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CanGaroo Envelopes labeled as the following: 1. CanGaroo Envelope (Large)...
The Issue: Possible suture brittleness or breakage along the Envelope seam before the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500...
The Issue: Incorrect labeling on the products package. The label on the package shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.