Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,047 recalls have been distributed to Idaho in the last 12 months.
Showing 13841–13860 of 27,833 recalls
Recalled Item: Arrow¿ PICC with Chlorag+ard Technology Product Code: CDC 44052 HPK1A...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ PICC Kit Product Code: ASK 45541 LVH1 Recalled by Arrow International...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC Kit pre loaded with Arrow¿ VPS Precision Stylet Recalled by Arrow...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central...
The Issue: Lidstock states the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Kwart Retro-Inject Ureteral Stent Set: PRODUCT/CATALOG NUMBER/GPN: 4.7...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Salle Intraoperative Pyeloplasty Stent Set PRODUCT/CATALOG NUMBER/GPN:...
The Issue: Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...
The Issue: Possibility that a suture raw material containing high endotoxin levels was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...
The Issue: System software inhibits the monitor and as a result does not measure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...
The Issue: Reports of aspirating biopsy needle breakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace PACS 4.4 Recalled by Philips Healthcare Informatics, Inc. Due...
The Issue: Images may potentially become corrupt while using the system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge-T 22706 SAMPLE MANIFOLD Material:701054912 Recalled by Maquet...
The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361 Recalled by Maquet...
The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.