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. 1,911 recalls have been distributed to Virginia in the last 12 months.
Showing 26341–26360 of 53,829 recalls
Recalled Item: Bronchofiberscope BF-P40 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-P180 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-MP160F Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 11 mm x 340 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-3C40 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-P60 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-1T60 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...
The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airway Mobilescope MAF-TM Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-XT40 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-160 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-XP60 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-XP40 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-Q180-AC Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 130 11 mm x 340 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...
The Issue: Two units in distribution were found to be mislabeled on the vial cap with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 400 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-Q180 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 13 mm x 260 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofibercope BF-6C240 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.