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. 1,943 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,943 in last 12 months

Showing 1912119140 of 29,425 recalls

Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· C.R. Bard, Inc.

Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to Misbranded: Product...

The Issue: Misbranded: Product labeled, Not made with natural rubber latex, may in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· PerkinElmer Life and Analytical Sciences, Wallac, OY

Recalled Item: Specimen Gate Laboratory Recalled by PerkinElmer Life and Analytical...

The Issue: Potential for errors in patient results generated by the Specimen Gate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2017· Ulrich Medical USA Inc

Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...

The Issue: Surgical technique was revised to prevent static plate screws blocking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...

The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Saline Dressing 8' x 4 (20.3cm x10.2 cm) Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Sodium Chloride Dressing Recalled by Covidien LLC Due to...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that in isolated cases when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip Recalled by...

The Issue: Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Verathon Inc

Recalled Item: It is recommended for patients with weight/size between 4-22 lbs Recalled by...

The Issue: Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged...

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

Class II — Potential Health HazardOngoing