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. 1,942 recalls have been distributed to Idaho in the last 12 months.
Showing 7041–7060 of 48,215 recalls
Recalled Item: SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIBIAL BEARING INSERT SERIES P-S I ASSY Intended for knee Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DUR PCA MTK REV INS LFT Intended for knee replacement Recalled by Howmedica...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #9 -Intended for knee Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #7 -Intended for knee Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DUR PCA MTK REV INS LFT Intended for knee replacement Recalled by Howmedica...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number:...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM)...
The Issue: The software application on the Programmer/Recorder/Monitor (PRM) for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod 5 App (on compatible Android smartphones) Recalled by Insulet...
The Issue: The bolus calculator is not recording the decimal point if it is the first...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT 7500 Recalled by Philips North America Llc Due to Multiple...
The Issue: Multiple software issues that affect device functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.