Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,542 recalls have been distributed to Maine in the last 12 months.
Showing 5021–5040 of 27,655 recalls
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: DUR PCA MTK REV INS RT 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 U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708...
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: 73-3910...
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: 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: SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0510...
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: SERIES II TIBIAL BEAR INSERT-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: SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #5 -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 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: SCORPIO TS TIB INSERT. Intended for knee replacement Part Number: 72-4-7518...
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 replacment Part Number: 72-4-7516...
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: LARGE PRIMARY REV.TIB.INSERT- DURACON 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: SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S Recalled by...
The Issue: Olympus identified inconsistencies in the Instructions for Use regarding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508...
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-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for 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: DURATION A-P LIPPED TIB.INSERT-DURAC 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: 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: 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.