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. 2,828 recalls have been distributed to Virginia in the last 12 months.
Showing 4461–4480 of 29,425 recalls
Recalled Item: Sterile convenience kit: Medline Birthing Room Pack Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prelude Guide Sheath Roadster Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Their is a potential that sheaths labeled with .018 dilators may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile convenience kits: a. Medline Delivery Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: Medline Open Heart CDS Recalled by MEDLINE...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioZorb Marker-BioZorb 3D Bioabsorbable Marker-Intended Use radiographic...
The Issue: Safety Information: Complaints describe complications/adverse events that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron3 - IVD use in the quantitative measurement Recalled by...
The Issue: Potential for falsely elevated Chol_2, LDLC, and Trig_2 results on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System AS Tibial Bearing / DCM ArCom Recalled by Biomet, Inc....
The Issue: Possible damage to the Vanguard Knee System AS Tibial Bearing caused during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Cart Recalled by Intuitive Surgical, Inc. Due to Surgical system may...
The Issue: Surgical system may have inadequately welded top and/or bottom belts in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology Recalled...
The Issue: Product incorrectly labelled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 Recalled by Philips North America Llc Due to Patient support table...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T S Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 1.5T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T for PET Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.