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. 979 recalls have been distributed to Virginia in the last 12 months.
Showing 40541–40560 of 53,829 recalls
Recalled Item: WIZARD2 5-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex ARC Hip Stem Recalled by Omnilife Science Inc. Due to Product may...
The Issue: Product may breach the inner and outer sterile pouches during shipping or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Multiple dietary supplement regulation violations.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tri-Mix (17.7 mg/0.59 mg/6 mcg) Injectable Recalled by The Compounding...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix (6.9/0.575/39.375) Injectable Recalled by The Compounding Pharmacy...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix Super Injectable Recalled by The Compounding Pharmacy of America Due...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 25 mg Recalled by The Compounding Pharmacy of America Due to Lack...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipovicine Modified II Injectable Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix MEDIUM (15 mg/0.5 mg/5 mcg) Injectable Recalled by The Compounding...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 8 mg Recalled by The Compounding Pharmacy of America Due to Lack...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix (37.5 mg/1.5 mg/50 mcg) Injectable Recalled by The Compounding...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 17 Recalled by The Compounding Pharmacy of America Due to Lack of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix T-106/PGE 2 0.1/0.14 Injectable Recalled by The Compounding Pharmacy...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methionine 25 mg/ml + Inositol 50 mg/ml + Choline 50 mg/ml Injectable...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.