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. 956 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
956 in last 12 months

Showing 46001–46020 of 53,829 recalls

DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2014· Actavis Laboratories, FL, Inc.

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...

The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2014· Teva Pharmaceuticals USA

Recalled Item: QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA...

The Issue: Defective Delivery System; defective valve

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 23, 2014· Elekta, Inc.

Recalled Item: Synergy XVI Intended for radiation therapy treatment. Recalled by Elekta,...

The Issue: XVI can incorrectly calculate the target position of the treatment table.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· CareFusion 303, Inc.

Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...

The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...

The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Heraeus Kulzer, LLC.

Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...

The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...

The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) Recalled...

The Issue: Software issues with ACUSON SC2000 ultrasound with software version 3/5...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2014· C P Medical Inc.

Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...

The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodApril 23, 2014· Miami Interculinary Center, Inc.

Recalled Item: Floribbean Key Lime Calypso Dip 12.5 oz Floribbean 68 SW 40 St. Suite 411...

The Issue: During an FDA inspection a product was found that the label fail to declared...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 22, 2014· Hamilton Medical, Inc.

Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....

The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 22, 2014· Biomet, Inc.

Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...

The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 22, 2014· SigmaPharm Laboratories LLC

Recalled Item: Liothyronine Sodium Tablets Recalled by SigmaPharm Laboratories LLC Due to...

The Issue: Cross Contamination with Other Products: Four lots of Liothyronine Sodium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2014· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Nylon fibers found in a bottle of 0.9%...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2014· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 21, 2014· Bausch & Lomb Inc- Greenville Solutions Plant

Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...

The Issue: Out of specification results for one of the two disinfectants.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodApril 21, 2014· Wegmans Food Markets, Inc.

Recalled Item: Scale label printed with "EASTER BREAD NET WT 17oz (1.06lb)" Recalled by...

The Issue: Wegmans Food Markets, Inc. has initiated a voluntary recall of all Wegmans...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing