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. 1,096 recalls have been distributed to Virginia in the last 12 months.
Showing 13141–13160 of 53,829 recalls
Recalled Item: JIF NATURAL PEANUT BUTTER packaged in 0.64oz and 96 count Recalled by The JM...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 40 OUNCE NATURAL HONEY Recalled by The JM Smucker Company LLC Due to...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dawn's Smoked Gouda & Bacon Potato Salad Recalled by Morski Brands, Inc. Due...
The Issue: Foreign object (metal).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 1.5 oz NATURAL CREAMY PEANUT BUTTER TO GO packaged in 8 and 36 count...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis) Recalled by Agilent...
The Issue: Label provided for substrate vail contained incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Item Number: 800774001 Recalled by ROi CPS LLC Due to A nonsterile...
The Issue: A nonsterile component was packaged in a sterile convenience kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Icono Recalled by Siemens Medical Solutions USA, Inc Due to During...
The Issue: During system tests, an increased wearing of the Image acquisition system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System...
The Issue: Potential for stent dislodgement and associated failures related to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...
The Issue: Complaints relating to urine output measurement accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension LTNI -In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension CTNI-In vitro diagnostic test intended to quantitively measure...
The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MODULAR CATHCART FRACTURE HEAD HIP BALL Recalled by DePuy Orthopaedics, Inc....
The Issue: The Cathcart Ball has an inherent +5mm offset which is not currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 Recalled by...
The Issue: There is a potential for sporadic incidents of positive and negative biases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glycopyrrolate Injection Recalled by Nephron Sterile Compounding Center LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate in 0.9% Sodium Chloride Injection Recalled by Nephron...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate Injection Recalled by Nephron Sterile Compounding Center LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.