Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,691 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,691 in last 12 months

Showing 51015120 of 29,298 recalls

Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Olympus Corporation of the Americas

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

Class II — Potential Health HazardOngoing