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. 2,828 recalls have been distributed to Virginia in the last 12 months.
Showing 5001–5020 of 29,425 recalls
Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...
The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...
The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: New warnings are being added to the Instructions for Use for all affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: IFU has been updated to include warnings about the risk of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: TruScan Body Recalled by TruAbutment Inc. Due to Retroactive:...
The Issue: Retroactive: Due to defect and quality issues dental scanner may not scan...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...
The Issue: X-ray exposure termination audible signal on Senographe Pristina with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...
The Issue: Knee batteries may need replacement with conforming batteries to ensure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSelect 5/16" Amber Latex Elastics-Intended use is orthodontics Recalled...
The Issue: Latex elastic bands were labeled as non-latex elastic bands, an allergic rx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Article No. NA6050411 Recalled by Ivoclar Vivadent, Inc. Due to Affected...
The Issue: Affected product may not perform as expected; the amalgam powder may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item...
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TERUMO HydroPearl Compressible Microspheres for Embolisation Recalled by...
The Issue: Due to, during the manufacturing process, the prescribed manufacturing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)...
The Issue: Level 3 masks were produced on alternate non-validated production equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CULTURE COLLECTION KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.