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. 2,803 recalls have been distributed to Virginia in the last 12 months.
Showing 9641–9660 of 29,425 recalls
Recalled Item: Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by...
The Issue: Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANCILLARY ADULT 140-DOSE CONVENIENCE KIT Recalled by Mckesson...
The Issue: Two unsuitable 3mL syringes with conventional needles for vaccine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN RANEY SCALP CLIPS-Disposable cylindrical clips designed to provide...
The Issue: Packaging-pouches with wrinkles across the Tyvek side may compromise the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSSUR MIAMI J SELECT COLLAR - Product Usage: is intended Recalled by Ossur...
The Issue: Due to insufficient column strength of the racks for all load conditions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Four Birthing Bed-used as a birthing bed for women Recalled by...
The Issue: Latch mechanism on the Lift-Off foot section of the Affinity Four Birthing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte...
The Issue: May show unexpected locus specific signals in addition to those at 19p13.3....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...
The Issue: The devices have a different inner diameter than the diameter specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann SCS Screwdriver Recalled by Straumann USA LLC Due to Tip of the...
The Issue: Tip of the screwdriver does not have the correct configuration / profile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...
The Issue: The devices have a different inner diameter than the diameter specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Product...
The Issue: Product distributed for use as an In-vitro Diagnostics without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60...
The Issue: Telepack may not power on when using the 3AA battery cradle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Cell Marque Corporation Due to Product distributed...
The Issue: Product distributed for use as an In-vitro Diagnostics without FDA clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno- angiography systems developed for single and biplane diagnostic...
The Issue: Software error VE10B -In case of a fault within the drivetrain of an axis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion systems with software release R1.x Recalled by PHILIPS MEDICAL...
The Issue: In the Azurion system, the user can add a new study to a patient by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion systems with software release R2.0.x Recalled by Philips Healthcare...
The Issue: In the Azurion system, the user can add a new study to a patient by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235-Proton Therapy System Recalled by Ion Beam Applications S.A. Due...
The Issue: if the user forgets to select the trigger input manually while beam gating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...
The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave 3 cc/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC Due...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.