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. 2,500 recalls have been distributed to West Virginia in the last 12 months.
Showing 11181–11200 of 27,884 recalls
Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...
The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AM1054 Randox Ammonia (NH3) Recalled by RANDOX LABORATORIES, LTD. Due to...
The Issue: Randox Ammonia reagents are being recalled from the field due to a positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AM1015 Randox Ammonia (NH3) Recalled by RANDOX LABORATORIES, LTD. Due to...
The Issue: Randox Ammonia reagents are being recalled from the field due to a positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.