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. 2,380 recalls have been distributed to West Virginia in the last 12 months.
Showing 23501–23520 of 27,884 recalls
Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...
The Issue: Loosened monitor arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX 1200 Compounder Recalled by Baxter Healthcare Corp. Due to If the...
The Issue: If the universal ingredient (UI) in an active configuration is changed using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O....
The Issue: ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coat-A-Count Direct Androstenedione Recalled by Siemens Healthcare...
The Issue: The assay is demonstrating a higher frequency of results greater than 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Auto-reader. Model numbers 390 Recalled by 3M Company - Health...
The Issue: Labeling on units shipped prior to May 16th, 2014 did not contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to Laser...
The Issue: Laser aperture label was not affixed to device prior to shipment in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Toe Instrument Kit Recalled by Arthrosurface, Inc. Due to An oversight...
The Issue: An oversight in the implementation of the design change record resulted in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hospira MedNet Medication Management Suite (MMS). Product Usage: The...
The Issue: Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 Recalled by...
The Issue: When liquid comes in contact with the DX-D 100 touch screen, the device may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Canto and associated Fluidics Cart Product Usage: Flow Recalled by...
The Issue: Laser cooling fans and internal fan of the associated fluidics cart are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...
The Issue: In certain circumstances, a software error can lead to a situation where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...
The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.