Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,614 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,614 in last 12 months

Showing 1236112380 of 28,172 recalls

Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Carroll-Baccari, Inc.

Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...

The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Philips North America, LLC

Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...

The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2019· Zimmer Biomet, Inc.

Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...

The Issue: Potential for the expiration date on the outer label that was applied by...

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 Architect 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 Pioneer 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 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