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. 1,849 recalls have been distributed to Virginia in the last 12 months.
Showing 35701–35720 of 53,829 recalls
Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...
The Issue: Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego Recalled by Siemens Medical Solutions USA, Inc Due to Due...
The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jakes Candy Gummies Worms. o Product label(s): ***Jakes Candy *** Recalled...
The Issue: Four Brothers Packaging, Inc.dba Jake's Candy is voluntarily recalling Gummy...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jakes Candy Assorted Starlight Kisses Recalled by Four Brothers Packaging...
The Issue: Four Brothers Packaging, Inc.dba Jake's Candy is voluntarily recalling...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jakes Candy Assorted Jelly Fruit Slices Recalled by Four Brothers Packaging...
The Issue: Four Brothers Packaging, Inc.dba Jake's Candy is voluntarily recalling...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bard TruGuide Disposable Coaxial Biopsy Needle Mixed Product Part Recalled...
The Issue: May contain two trocar tip stylets with coaxials or two blunt tip stylets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPHERICAL HEAD (R) 6.5 MM CANCELLOUS SCREW Recalled by Smith & Nephew, Inc....
The Issue: The labels correctly state that the product should be a 25mm screw, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bulk flour bland breader packaged into 15 Recalled by Newly Weds Foods Inc...
The Issue: Flour contaminated with E. coli O121 was used in the manufacuring of flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Optilite Freelite Lambda Free Kit Product Code: LK018.OPT Recalled by The...
The Issue: Batch numbers listed are reporting Lambda Free Light Chain results >114mg/L...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...
The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...
The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...
The Issue: Issue with design specification; oversized condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...
The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.