Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,521 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,521 in last 12 months

Showing 49614980 of 27,157 recalls

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 4, 2023· Shirakawa Olympus Co., Ltd.

Recalled Item: Model No. CYF-V2 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. CYF-VH 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. 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-XP190 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus...

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. CYF-V2R 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. 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· 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· Shirakawa Olympus Co., Ltd.

Recalled Item: Model No. CYF-5 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. ENF-XP 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 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