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

53,829 total recalls
916 in last 12 months

Showing 52041–52060 of 53,829 recalls

Medical DeviceSeptember 5, 2012· Zimmer, Inc.

Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...

The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿-PT lateral proximal 3 hole tibial plate Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Sirus¿ intramedullary nail for tibia Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Universal spacer 6-45 Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Set screw M6 Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Revision Humeral stem Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Metasul¿ Durom¿ Femoral component Sterile Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿-PH Plate Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30 Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30¿ Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Biolox¿ delta Ceramic Femoral Head Rx only Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard Ventralight ST Mesh. - Ellipse 7" x 9" (17.8 Recalled by Davol, Inc.,...

The Issue: Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Alloclassic¿ SL-Offset Stem sterile Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ L.I.S. Stabilizing cord Rx Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile Recalled by...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30¿ Distal centralizer Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Humeral stem Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing