Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,673 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,673 in last 12 months

Showing 50815100 of 29,186 recalls

Medical DeviceDecember 4, 2023· Shirakawa Olympus Co., Ltd.

Recalled Item: Model No. CYF-5R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...

The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2023· Olympus Corporation of the Americas

Recalled Item: Soltive SuperPulsed Laser System TFL Fiber Stripper Recalled by Olympus...

The Issue: The strippers and cleavers are provided non-sterile and labelled as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2023· Shirakawa Olympus Co., Ltd.

Recalled Item: Model No. CYF-VHR Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...

The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2023· Shirakawa Olympus Co., Ltd.

Recalled Item: Model No. BF-P190 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...

The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2023· Olympus Corporation of the Americas

Recalled Item: Soltive SuperPulsed Laser System TFL FIBER CLEAVER Recalled by Olympus...

The Issue: The strippers and cleavers are provided non-sterile and labelled as...

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: 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: 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-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 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: SCORPIO TOTAL KNEE CONCENTRIC 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: SCORPIO TOTAL KNEE CONCENTRIC 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· Howmedica Osteonics Corp.

Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110...

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: 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 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