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. 1,936 recalls have been distributed to Virginia in the last 12 months.
Showing 22141–22160 of 29,425 recalls
Recalled Item: Battery Power Line II Battery Oscillator Recalled by The Anspach Effort,...
The Issue: Has the incorrect operating directions on the mode switch ring, i.e. its is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...
The Issue: The firm was notified by some of their customers that some of the sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Preformance Post Dental implants Recalled by Biomet 3i, LLC Due to Pouches...
The Issue: Pouches may not have been sealed during packing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...
The Issue: Potential for separation of the proximal handle from the shaft.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System. Used to manage workflows for treatment...
The Issue: First Databank (FDB) is a third party product incorporated into MOSAIQ. FDB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona EM Proximal Tube Recalled by Zimmer, Inc. Due to Complaints that the...
The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona EM Distal Rod Recalled by Zimmer, Inc. Due to Complaints that the...
The Issue: Complaints that the ratchet teeth of the tube are not latching onto the rod.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cournand Modified 2-PC 19G Recalled by Stryker Instruments Div. of Stryker...
The Issue: The Guidewire Introducer Needle (0910-192-000) was shipped after the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Tower is the input device to program the Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ZYTO Select and ZYTO Elite software programs are used Recalled by ZYTO...
The Issue: ZYTO Technologies Inc. Announces a Voluntary Recall of the ZYTO Tower and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30 deg Recalled by Intuitive Surgical, Inc. Due to This correction to the da...
The Issue: This correction to the da Vinci Xi I&A User Manual communicates proper use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of...
The Issue: "The public reason for the recall is that the product is being recalled out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO¿ Warming Cabinet. Manufactured by: STERIS Corporation To raise the...
The Issue: The firm discovered that information printed on the quick magnet is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 Recalled by Boston...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS Recalled by...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve Recalled by Boston Scientific Corp...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization...
The Issue: These screws have a single lead (instead of a triple lead) thread. The screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number:...
The Issue: During routine monitoring of complaints, BSC noted that the IntellaTip MiFi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW...
The Issue: Due to the potential for reporting erroneous results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.