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. 1,768 recalls have been distributed to Virginia in the last 12 months.
Showing 51381–51400 of 53,829 recalls
Recalled Item: Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable...
The Issue: Zimmer is initiating a lot specific recall because affected lots could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EstroGel (estradiol gel) 0.06% Recalled by Ascend Therapeutics Inc Due to...
The Issue: Defective Container: Pump head detaching from the canister unit upon removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cocoa~Latte Hot Drink Maker Recalled by Focus Products Group Llc Due to The...
The Issue: The Cocoa~Latte Hot Drink Maker was manufactured with a small brass metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dried Golden Raisins 8 oz Recalled by Whole Alternatives Llc Due to...
The Issue: Undeclared sulphur dioxide
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dried Apricots 6 oz Recalled by Whole Alternatives Llc Due to Undeclared Sulphur
The Issue: Undeclared sulphur dioxide
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chicken of the Sea Solid White Tuna in Water Recalled by Tri-Union Seafoods,...
The Issue: Chicken of the Sea is recalling Solid White Tuna in Water because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enterprise 9000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek 11 MM Fully Fluted Reamer Recalled by DePuy Mitek, Inc., a...
The Issue: Specific units of the DePuy Mitek Sterile Reamers are not labeled correctly,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 8000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...
The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Praxair Vantage Grab n Go - Gas Cylinder pressure regulator Recalled by...
The Issue: Isolated incidents of ignition inside Grab n' Go cylinders that had been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phenobarbital Recalled by Abbott Laboratories, Inc Due to...
The Issue: Abbott Diagnostics is recalling Clinical Chemistry Phenobarbital reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...
The Issue: There is a potential for data loss associated with empty path names...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity PACS Workstation Recalled by GE Healthcare It Due to While...
The Issue: While merging exams in a test instance, merges carry forward in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particulate and particulate embedded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biomet Offset Tibial Tray 2.5 mm Adaptor Recalled by Biomet, Inc. Due to...
The Issue: Biomet investigation identified that the square end of the offset tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viterion TeleHealth Monitor Model Number V100 Recalled by Viterion...
The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viterion TeleHealth Monitor Model Number V500 Recalled by Viterion...
The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viterion TeleHealth Monitor Model Number V100-BGM Recalled by Viterion...
The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEG NeuroAmp Recalled by EEG Info Due to Mislabeling
The Issue: EEG Info, Inc. is recalling the EEG Neuroamp device because they have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...
The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.