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. 2,359 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,359 in last 12 months

Showing 4708147100 of 49,744 recalls

FoodJanuary 16, 2013· Bimbo Bakeries Usa

Recalled Item: Publix Premium Bagels Recalled by Bimbo Bakeries Usa Due to The firm found...

The Issue: The firm found metal fragments in two packages of product.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 16, 2013· Bimbo Bakeries Usa

Recalled Item: Sara Lee Deluxe Bagels Recalled by Bimbo Bakeries Usa Due to The firm found...

The Issue: The firm found metal fragments in two packages of product.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 16, 2013· Bimbo Bakeries Usa

Recalled Item: Thomas' Bagels Recalled by Bimbo Bakeries Usa Due to The firm found metal...

The Issue: The firm found metal fragments in two packages of product.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 16, 2013· Bimbo Bakeries Usa

Recalled Item: Weight Watchers 6 Original Bagels Recalled by Bimbo Bakeries Usa Due to The...

The Issue: The firm found metal fragments in two packages of product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...

The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...

The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Philips BuckyDiagnost Radiographic Recalled by Philips Healthcare Inc. Due...

The Issue: An inspection shows several IATDs (Installation Acceptance Test could not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...

The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage:...

The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Iconos R200 C20 Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens has become aware of a potential malfunction and possible hazard to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2013· DePuy Spine, Inc.

Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 11C Plus KIT Catalog Number: Recalled...

The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2013· DePuy Spine, Inc.

Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM KIT Catalog Number: 283913000....

The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2013· DePuy Spine, Inc.

Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 7CC KIT Catalog Number: 283907000....

The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2013· DePuy Spine, Inc.

Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Catalog Number:283905000....

The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2013· Del Mar Reynolds Medical, Ltd.

Recalled Item: Spacelabs BleaseSirius Anesthesia Workstation Recalled by Del Mar Reynolds...

The Issue: A defect in CAS I/II Absorbers in the Spacelabs Anesthesia Workstations and...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 14, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Senographe Essential System. The Senographe 2000D system...

The Issue: GE Healthcare has recently become aware of a potential issue due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2013· Atricure Inc

Recalled Item: Atricure Inc. Recalled by Atricure Inc Due to Products from lot no. 41865...

The Issue: Products from lot no. 41865 may have been sent out with Incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2013· Ansell Healthcare Products LLC

Recalled Item: LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell...

The Issue: Out of an abundance of caution, Ansell is implementing a voluntary recall of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2013· Breg Inc

Recalled Item: BREG Sterile Polar Pads Recalled by Breg Inc Due to The recall was initiated...

The Issue: The recall was initiated because Breg has determined that some Sterile Polar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 14, 2013· Philips Healthcare Inc.

Recalled Item: Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and...

The Issue: VS2+ screen may lock up and stop monitoring during patient use

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

Class II — Potential Health HazardOngoing