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. 1,090 recalls have been distributed to Virginia in the last 12 months.
Showing 14841–14860 of 29,425 recalls
Recalled Item: EMPOWR Locking Femoral Impactor Recalled by Encore Medical, Lp Due to The...
The Issue: The firm has received reports/complaints concerning the breakage of the tips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...
The Issue: The products were manufactured without a back bevel on the needle tip. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL Luer-Lok Syringe Recalled by Becton Dickinson & Company Due to The...
The Issue: The syringes have scale markings that were printed incorrectly. The scale is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL Safety-Lok Syringe Recalled by Becton Dickinson & Company Due to The...
The Issue: The syringes have scale markings that were printed incorrectly. The scale is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...
The Issue: Potential for the Semi-Rigid canister lid to fragment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...
The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velofix SA cervical cage Recalled by U&I CORP. Due to The vertical...
The Issue: The vertical dimensions of screw-hole position in some standalone cages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TASE 500 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...
The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TASE 400 Imaging systems Recalled by COLLINS AEROSPACE Due to the Nominal...
The Issue: the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kii Fios First Entry Recalled by Applied Medical Resources Corp Due to The...
The Issue: The product may not have met sterility requirements . Use of a non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX2 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX3 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX3 Elite Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Smart Disclosure System Recalled by Spacelabs...
The Issue: Several reports were received that patient records were printed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON NX2 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: The action is being initiated due to internal testing which identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium-ion Rechargeable Batteries for the Philips MX40 Wearable Monitor by...
The Issue: Lithium-ion Rechargeable Batteries for the Philips MX4O Wearable Monitor may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.