Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,591 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,591 in last 12 months

Showing 1228112300 of 28,355 recalls

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: 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: 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: 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: 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: 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 with FlexTip Plus Catheter 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: 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: 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