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. 1,936 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,936 in last 12 months

Showing 2130121320 of 29,425 recalls

Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P3 Lambswool. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Sorbatex. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Ossur H / F

Recalled Item: Ossur Lil Angel Vest P2 Lambswool. Pediatric sized vest is Recalled by Ossur...

The Issue: There is a potential for partial or complete fracture of the plastic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV Intermediate Safety MST Kit under the Recalled by...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...

The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Vaxcel PICC with PASV MST-60 Kit under the following labels: 1) 3F Recalled...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2016· Navilyst Medical, Inc., an AngioDyamics Company

Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...

The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After importing segmentation results of the left atrium created on the Artis...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· Integra York PA, Inc

Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...

The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· RESEARCH INSTRUMENTS LTD - SITE B

Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...

The Issue: The units have been fitted with a potentially faulty power supply cable.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2016· Integra LifeSciences Corporation

Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...

The Issue: Integra's post QA release review of historical product release test results...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Repro-Med Systems, Inc.

Recalled Item: HIgH-Flo Subcutaneous Safety Needle Sets Recalled by Repro-Med Systems, Inc....

The Issue: On 2/24/2016 during post sterilization inspection of part number F180...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Ferno-Washington Inc

Recalled Item: Poly-bags containing splint strap labeled with "Pediatric" sticker. Each...

The Issue: On March 9, 2016, the firm was contacted regarding the possibility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Repro-Med Systems, Inc.

Recalled Item: Freedom60 Precision Flow Rate Tubing Sets Recalled by Repro-Med Systems,...

The Issue: On 2/24/2016 during post sterilization inspection of part number F180...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Ferno-Washington Inc

Recalled Item: Poly-bags containing the strap labeled with "Adult" sticker. Each strap...

The Issue: On March 9, 2016, the firm was contacted regarding the possibility of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing