Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 987 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
987 in last 12 months

Showing 18421–18440 of 46,762 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: 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
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: 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 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 Set 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 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 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· Cardinal Health 200, LLC

Recalled Item: Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 Recalled by...

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
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
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 Recalled by...

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
Medical DeviceJanuary 15, 2020· Cardinal Health 200, LLC

Recalled Item: Monoject Bluntfill with Filter Recalled by Cardinal Health 200, LLC Due to...

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
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