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. 1,047 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,047 in last 12 months

Showing 20841–20860 of 53,829 recalls

Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: 10 cc Luer-Slip Loss of Resistance Syringe Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Kit Recalled by Arrow...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Bard Peripheral Vascular Inc

Recalled Item: BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth...

The Issue: The catheter locks for the lot may contain an 8Fr catheter lock instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...

The Issue: There is the potential for various failures with the LOR (loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject 3mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...

The Issue: Non-sterile product was shipped to customers. Product package is labeled as...

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

Class II — Potential Health HazardOngoing