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. 2,614 recalls have been distributed to Idaho in the last 12 months.
Showing 1921–1940 of 27,833 recalls
Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...
The Issue: The battery for certain ultrasound systems can potentially develop an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Coracoid Clamp Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Glenoid Digitizer Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Depth Stop Pin Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Instrument Kit Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Box Base Recalled by Tornier S.A.S. Due to...
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless...
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Instrument Check Block Recalled by Tornier...
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker HoloBlueprint Application Recalled by Tornier S.A.S. Due to Stryker...
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...
The Issue: Medline ReNewal has identified that the drip chambers of affected devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker Blueprint Mixed Reality Glenoid Box Lid Recalled by Tornier S.A.S....
The Issue: Stryker identified an elevated complaint rate related to difficulties using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...
The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.