Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,778 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,778 in last 12 months

Showing 50815100 of 29,154 recalls

Medical DeviceDecember 1, 2023· Howmedica Osteonics Corp.

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.

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

Recalled Item: SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032...

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: 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.

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

Recalled Item: DURATION PLASTIC PATELLA-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 replacement Part Number:72-4-7512...

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: 72-4-7524...

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: 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.

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· 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: 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-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: 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: 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 TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee...

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. 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: 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: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710...

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