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. 2,058 recalls have been distributed to Kentucky in the last 12 months.
Showing 5741–5760 of 28,748 recalls
Recalled Item: Arrow ErgoPack Pressure Injectable One-Lumen PICC Recalled by ARROW...
The Issue: This recall has been initiated due to reports that the product code and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture Recalled by ETHICON, LLC Due...
The Issue: Internal testing on returned product from this lot confirmed that some PDS"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit -...
The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software update corrected an issue where "low" and "terminal" battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...
The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10ML SYRINGE LUER LOCK W/OUT NEEDLE Recalled by Fresenius Medical Care...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...
The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...
The Issue: Centered glenosphere box may contain an eccentric glenosphere.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10ML SYRINGE LUER LOCK W/NEEDLE Recalled by Fresenius Medical Care Holdings,...
The Issue: There is a potential for blood backfill leakage and foreign material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prucka 3 Amplifiers Recalled by GE Medical Systems Information Technologies...
The Issue: A diode on the power supply of the Prucka 3 Amplifier used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartmate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to Inability to...
The Issue: Inability to start and/or complete the coring procedure due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B.Braun NORM-JECT Luer Lock Solo Recalled by B. Braun Medical, Inc. Due to...
The Issue: The sterile blister packaging may be damaged, and sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with...
The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.