Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,725 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,725 in last 12 months

Showing 1266112680 of 29,154 recalls

Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: PICC Set- PR-35052-HPHNM Recalled by Arrow International Inc Due to Product...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1 Recalled by...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow Central Venous Catheterization Kit ASK-04200-UPM Recalled by Arrow...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT JH-05500 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM Recalled by...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC Recalled by...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT YC-02220 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 Recalled by Arrow...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN Recalled by...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: (1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") Recalled by Arrow...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT CK-02220 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow Maximal Barrier Drape ASK-00002-1A Recalled by Arrow International Inc...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT AM-05500 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow SPINAL ANESTHESIA SET ASA-25090-S Recalled by Arrow International Inc...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL NEEDLE KIT SL-05500 Recalled by Arrow International Inc Due...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Arrow International Inc

Recalled Item: Arrow EPIDURAL NEEDLE COMPONENT AN-05505 Recalled by Arrow International Inc...

The Issue: Product lidstock contains the incorrect expiration date for the product

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The potential exists for system movement to be permanently blocked by an...

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

Class II — Potential Health HazardOngoing