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. 1,850 recalls have been distributed to Virginia in the last 12 months.
Showing 32841–32860 of 53,829 recalls
Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...
The Issue: The Pause function on central monitors will not automatically resume when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian...
The Issue: Defective Delivery System; reports of the device failing to activate which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg Recalled by Meridian...
The Issue: Defective Delivery System; reports of the device failing to activate which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluconazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars Recalled by Nestle USA...
The Issue: Firm received two complaints of finding a Haagen-Dazs Vanilla Milk Almond...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...
The Issue: Product shipped proximate to or past the expiration date listed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...
The Issue: Improperly rated fuses were used in the manufacture of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: CUSTOM CADAVER KIT 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.
Recalled Item: EYE KIT The Covidien Curity Oval Eye Pads are individually Recalled by...
The Issue: Centurion Medical Products is recalling Convenience Kits that contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: OPHTHALMIC DRS 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.