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. 2,609 recalls have been distributed to Kentucky in the last 12 months.
Showing 11221–11240 of 28,748 recalls
Recalled Item: ProScreen" Drugs of Abuse Test (AMT Item/ AMT Description): PSD-6MB/...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickTox Drug Screen DipCard(AMT Item/ AMT Description): QT70/ "QuickTox¿...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Check 2 Panel Drug Cup: (THC/COC) Recalled by Ameditech Inc Due to...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCup Dx14 Drug Screen Cup(AMT Item Number/ AMT Description):...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Check 14 Panel Drug Cup: (BMC style) Recalled by Ameditech Inc Due to...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein One Step + DOA Cup (AMT Item Number/ Recalled by Ameditech Inc...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDDA Drugs of Abuse Cup(AMT Item/ AMT Description): TDDA-6MBAU-CUP /"TDDA...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drug Screening Component: Uncut Sheets Part Number/ Description/ LOT Number...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Noble 1 Step+ Cup (AMT Item Number/ AMT Description): NBCA-13A-B Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Check 7 Panel Drug Cup: (AMP/COC/MDMA/MET/OPI/PCP/THC) Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToxCup Drug Screen Cup (AMT Item Number/ AMT Description): HT29A/"ToxCup¿...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UIBC Recalled by Beckman Coulter Inc. Due to The manufacturer has identified...
The Issue: The manufacturer has identified that the use of Unsaturated Iron Binding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consult Diagnostics Drugs Abuse Test Cup (AMT Item Number/ AMT Recalled by...
The Issue: Various immunoassay enzymes failed product performance, thereby the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Speed Stitch Needle Cassette Recalled by ArthroCare Corporation Due to Due...
The Issue: Due to a supplier error where a portion of the raw material was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM 830 Model # H3910AC Recalled by GE Healthcare, LLC Due to Rotor bearing...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery 670 DR Model # H3100BT Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Model # H3100AS Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia S-Series and Symbia T-Series - Product Usage: Intended use Recalled...
The Issue: This letter is to inform you of the possibility that your Symbia S or Symbia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 CZT Model # H3906CW Recalled by GE Healthcare, LLC Due to Rotor...
The Issue: Rotor bearing screws were found loose on detector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.