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. 2,581 recalls have been distributed to Idaho in the last 12 months.
Showing 6561–6580 of 27,833 recalls
Recalled Item: VentStar Bag Set (N) 110 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Watertrap (P) 180 w/oLL Recalled by Draeger Medical, Inc. Due to...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VentStar Coax (P) 150 Recalled by Draeger Medical, Inc. Due to Glued...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ID Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections of...
The Issue: Glued connections of the breathing circuit can become loose before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml Recalled by...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...
The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat...
The Issue: The product contains an expired diluent vial. If the impacted product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL (UVSL) Command Module Recalled by Spacelabs Healthcare, Inc....
The Issue: Command modules will display the following when parameter processing is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation Cranial Software Recalled by Medtronic Navigation, Inc. Due...
The Issue: During non-axial/some axial exams, software anomalies occur during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: Recalled by Bard...
The Issue: Coaxial cannula internal diameter and length of biopsy instruments exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture...
The Issue: The Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Over-Head Ceiling Tube Support Recalled by SHIMADZU CORPORATION MEDICAL...
The Issue: Eight fixing bolts at the base of the X-ray ceiling tube column assembly may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.