Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,543 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,543 in last 12 months

Showing 46614680 of 27,884 recalls

Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2024· Retractable Technologies, Inc.

Recalled Item: EasyPoint Needle Recalled by Retractable Technologies, Inc. Due to The...

The Issue: The needle cannula of a retractable needle may detach from the needle holder...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2024· Abbott Medical

Recalled Item: Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a...

The Issue: Their is a potential that electromagnetic interference may cause leadless...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2024· Beaver Visitec International, Inc.

Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...

The Issue: Pack and pouch label is missing the manufacturing and expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis LSI ATM (11q22.3) SpectrmOrange...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: Wash station: M1000 Wash Station Assembly & DITI Slide Recalled by Abbott...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 1, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedStation ES Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinets, running affected software, and Windows 10...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2024· Abbott Molecular, Inc.

Recalled Item: In-vitro diagnostic kits: (1) Abbott Vysis MDM2 / CEP 12 FISH Probe Kit...

The Issue: Products that were intended for export only which were not approved or...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 31, 2024· Technicality Inc.

Recalled Item: Trumpet Recalled by Technicality Inc. Due to The Ring on the Trump Needle...

The Issue: The Ring on the Trump Needle Guide can detach when excessive pressure is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD to calibrate the Microalbumin...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2024· Randox Laboratories Ltd.

Recalled Item: Microalbumin Calibrator Series (mALB CAL)-IVD used to calibrate the...

The Issue: Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO Recalled by Angiodynamics,...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2024· Angiodynamics, Inc.

Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....

The Issue: Non-conformance may prevent the guidewire from passing through the...

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

Class II — Potential Health HazardOngoing