Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,887 recalls have been distributed to Virginia in the last 12 months.
Showing 30181–30200 of 53,829 recalls
Recalled Item: BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 Recalled by...
The Issue: A limited portion of the lot was manufactured with less than the required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Product Usage: The Persona Partial Knee Recalled...
The Issue: Potential for the Persona Partial Knee Impactor Pad to fracture.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fortify VR - Model Numbers: CD1231-40 and CD1231-40Q Recalled by St Jude...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The device may exhibit...
The Issue: The device may exhibit premature battery depletion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...
The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...
The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...
The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Big Win Butter Popcorn Recalled by Dedinas Franzak Enterprises dba Cheeze...
The Issue: Dedinas Franzak Enterprises dba Cheeze Kurls Inc. initiated a voluntary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: When a prior study is being replaced in the workflow step, in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...
The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Choice Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP Deviations;...
The Issue: GMP Deviations; potential bacterial contamination may have been introduced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mild Healthcare Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP...
The Issue: GMP Deviations; potential bacterial contamination may have been introduced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option Systems Antibacterial Foaming Hand Wash Recalled by Inopak Ltd Due to...
The Issue: GMP Deviations; potential bacterial contamination may have been introduced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate tablets Recalled by Wockhardt Usa Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: 5mg strength being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Q Care Continue Care for the non-ventilated patient. Contains Recalled by...
The Issue: Cross Contamination With Other Products: Oral care solutions were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl Injection Recalled by Pfizer Inc. Due to Lack of sterility...
The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levophed (norepinephrine bitartrate) injection Recalled by Pfizer Inc. Due...
The Issue: Lack of sterility assurance: resulting from use of a damaged sterilizing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof-A (Acetaminophen 160 mg Recalled by Centurion Labs, LLC Due to...
The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Recalled...
The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.