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. 1,857 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
1,857 in last 12 months

Showing 2898129000 of 49,744 recalls

Medical DeviceMay 8, 2017· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: Merge PACS did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2017· Zimmer Biomet, Inc.

Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Durability characteristics of reusable instruments were not established

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Her2/Neu (c-erbB-2) (CB-1 1) Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· GE Healthcare, LLC

Recalled Item: Infant Warmer System (IWS) Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Innovasis, Inc

Recalled Item: Opteryx Variable Rescue Screw Recalled by Innovasis, Inc Due to Opteryx...

The Issue: Opteryx Variable Rescue Screws are engraved with incorrect (larger) size (16...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Alphatec Spine, Inc.

Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Recalled...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus I Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Her2/Neu (EP3) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Adenovirus (20/11 & 2/6) Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: CD117 Recalled by Cell Marque Corporation Due to Cell Marque has determined...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Estrogen Receptor (EP1) 7.0 mL Catalog number 249R-28 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18 Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
DrugMay 5, 2017· Genetic Edge Compounds LLC

Recalled Item: GEC LX Laxoplex 60 capsules Dietary Supplement Recalled by Genetic Edge...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 5, 2017· Ascend Laboratories LLC

Recalled Item: AMLODIPINE BESYLATE TABLET Recalled by Ascend Laboratories LLC Due to...

The Issue: PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodMay 5, 2017· Pinnacle Foods, LLC

Recalled Item: AUNT JEMIMA(R) LIL' GRIDDLES(TM) BLUEBERRY MINI PANCAKES Recalled by...

The Issue: Potential for Listeria monocytogenes contamination

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund