Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,621 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,621 in last 12 months

Showing 1264112660 of 29,186 recalls

Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· GE Healthcare, LLC

Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...

The Issue: It was identified that due to a potential installation workflow issue, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Lipase Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Firm has received customer complaints regarding failed calibrations and...

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 StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1 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) 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