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. 1,067 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,067 in last 12 months

Showing 16341–16360 of 29,425 recalls

Medical DeviceMay 21, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Digital PET/CT System Recalled by Philips Medical Systems...

The Issue: The block used to connect the patient pallet to the couch may be assembled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Qiagen Sciences, Inc.

Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...

The Issue: Potential for control line not appearing on the test strip

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 18, 2018· Guangzhou Wondfo Biotech Co., Ltd.

Recalled Item: TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO Recalled by Guangzhou...

The Issue: GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...

The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· OMNIlife science Inc.

Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...

The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Guangzhou Wondfo Biotech Co., Ltd.

Recalled Item: TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO Recalled by Guangzhou...

The Issue: GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2018· Guangzhou Wondfo Biotech Co., Ltd.

Recalled Item: TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO Recalled by Guangzhou...

The Issue: GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2018· Arrow International Inc

Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...

The Issue: Product pouch label may not easily identify the lot number, expiration date...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: DRILL PT GUIDE WIRE 2MM X 60CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: GUIDE WIRE w/ BALL TIP 2.0MMX98CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: RECON DRILL 6MM X 439MM Recalled by Zimmer Biomet, Inc. Due to The firm is...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: The Recalled by Abbott Laboratories, Inc Due to An update to the Reagents...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: BALL TIP GUIDE WIRE 3.2MMX55CM Recalled by Zimmer Biomet, Inc. Due to The...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: 3.2MM X 560MM COCR THD TIP Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Zimmer Biomet, Inc.

Recalled Item: G-PIN 2.8BL 3.2PL 98CM 2PK Recalled by Zimmer Biomet, Inc. Due to The firm...

The Issue: The firm is recalling various trauma guide wires due to insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2018· Abbott Laboratories, Inc

Recalled Item: C4 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...

The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...

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

Class II — Potential Health HazardOngoing