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. 2,594 recalls have been distributed to Idaho in the last 12 months.
Showing 4621–4640 of 27,833 recalls
Recalled Item: Nimbus II Infusion System Recalled by InfuTronix LLC Due to InfuTronix is...
The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...
The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral Recalled...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral Recalled by...
The Issue: Inability to advance the guidewire through the feeding tube during placement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALYARD SURGICAL HOOD Recalled by O&M HALYARD, INC. Due to Mislabeling
The Issue: Product was mislabeled as a Surgical Cap at its dispenser level.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kits that include High Crack Check Valve PN...
The Issue: Pressure relief valve included in certain lots of cardiovascular procedure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Tube Securement Device Recalled by 3M Company - Health Care Business Due...
The Issue: Manufacturing nonconformities are in some lots of the Tube Securement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific iSLEEVE EXPANDABLE Introducer Set Recalled by Boston...
The Issue: Boston Scientific is conducting a removal of specific batches of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Recalled...
The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Recalled...
The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec EsteemBody Soft Convex Recalled by ConvaTec, Inc Due to Convatec...
The Issue: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single...
The Issue: A deterioration of the cutting knife, including overheating and burning, can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus...
The Issue: A deterioration of the cutting knife, including overheating and burning, can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Ten 10ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Origio Sperm Wash Medium Pack of Five 60ml bottles - Recalled by...
The Issue: Low concentration of sodium pyruvate in the wash could compromise gamete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medivance Neonatal ArcticGel Pads Recalled by Medivance Inc. Due to Neonatal...
The Issue: Neonatal pads are experiencing reduced water flow, which may reduce or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.