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. 1,029 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,029 in last 12 months

Showing 14301–14320 of 48,376 recalls

Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: Stretch Leveller Model Number: 3156200 - The combination of this Recalled by...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: LikoStretch 1900 Model Number: 3156051 - The combination of this Recalled by...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC Recalled...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
DrugAugust 11, 2021· Ebay Seller - John Nguyen

Recalled Item: Hydro Pinapple Burn Max Health Thach Dua Recalled by Ebay Seller - John...

The Issue: Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodAugust 11, 2021· RMH Foods

Recalled Item: Gordon Choice Deli Style Tuna Salad Recalled by RMH Foods Due to Undeclared...

The Issue: Undeclared wheat and tuna

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 10, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Non-Sterility: firm's third party lab confirmed microbial contamination.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 10, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-single use Recalled by B. Braun...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Vitrectomy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ear Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Basic Cataract tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Newborn Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Core Biopsy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Stereotactic Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the pump set...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing