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. 2,590 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,590 in last 12 months

Showing 1488114900 of 28,172 recalls

Medical DeviceSeptember 18, 2018· Beckman Coulter Inc.

Recalled Item: The Access Cortisol Reagent. REF (Catalog Number) 33600 Recalled by Beckman...

The Issue: Cross contamination may have occurred between wells for the reagent pack. As...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2018· COVIDIEN LLC

Recalled Item: Puritan Bennett 980 (PB980) ventilator series: Puritan Bennett" 980...

The Issue: Software Update: External USB Drive performance and its impact on Graphic...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2018· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic Navigation 0-arm 02 Imaging System interventional fluoroscopic...

The Issue: O-arm 02 Imaging Systems correction to software version 4.1.0; new version...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Leica Microsystems, Inc.

Recalled Item: BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 Recalled by...

The Issue: The power supply unit for the printer used with the device can potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· BioMerieux SA

Recalled Item: NucliSENS¿ Magnetic Extraction Reagents Recalled by BioMerieux SA Due to...

The Issue: Data loggers showed that one shipment to the United States experienced low...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2018· Sterilmed, Inc.

Recalled Item: Reprocessed Agilis Steerable Introducer: indicated for introducing various...

The Issue: Reprocessed Agilis Steerable Introducers may not meet endotoxin requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE LOGIQ E10 Ultrasound System Recalled by GE Healthcare, LLC Due to There...

The Issue: There is a potential for an undetected over temperature condition on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MC Recalled by GE Healthcare, LLC Due to A detector...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MG Multi-Geometry Digital CSE Dual Detector Gamma...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Luminex Corporation

Recalled Item: VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as...

The Issue: Potential to lead to a false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· GE Healthcare, LLC

Recalled Item: GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH...

The Issue: A detector can detach and fall.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Camera Arm Drape (Box of 20) individually sealed in poly-Tyvek Recalled by...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2018· Ecolab Inc

Recalled Item: Disposable Accessory Kit Recalled by Ecolab Inc Due to The pouches of...

The Issue: The pouches of certain lots of product may have wrinkles along the pouch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2018· Roche Diagnostics Corporation

Recalled Item: CoaguChek¿ XS System Prothrombin time test: CoaguChek XS PT Test 2X24 Strips...

The Issue: Abnormally high INR test results with the affected CoaguChek test strips

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 13, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System Recalled...

The Issue: The service manual was not updated at the time of the release of software...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· CMP Industries, Llc

Recalled Item: IMPAK Elastic Acrylic Resin Liquid Heat Cure Type 1 Recalled by CMP...

The Issue: Foreign material in product

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 3000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing