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. 2,448 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,448 in last 12 months

Showing 3236132380 of 49,744 recalls

Medical DeviceJuly 20, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2016· Nobel Biocare Usa Llc

Recalled Item: Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Recalled by...

The Issue: Incorrect drill protocol in the Instructions for Use (IFU)

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

Class II — Potential Health HazardOngoing
DrugJuly 19, 2016· Talon Compounding Pharmacy

Recalled Item: Human Chorionic Gonadotropin Injection (a) 2500 iu Recalled by Talon...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2016· Talon Compounding Pharmacy

Recalled Item: Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection Recalled by Talon...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: Venlafaxine HCL ER Capsule USP Recalled by Zydus Pharmaceuticals USA Inc Due...

The Issue: Failed Dissolution Specifications: out of specification dissolution results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 19, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: Venlafaxine HCL ER Capsule USP Recalled by Zydus Pharmaceuticals USA Inc Due...

The Issue: Failed Dissolution Specifications: out of specification dissolution results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 19, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...

The Issue: Sterility compromised due to breach in sterile packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: MultiDiagnost Eleva Recalled by Philips Electronics North America...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: UroDiagnost Recalled by Philips Electronics North America Corporation Due to...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2016· Philips Electronics North America Corporation

Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...

The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...

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

Class II — Potential Health HazardOngoing
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Ointment Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Nasal Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2016· GlaxoSmithKline, LLC

Recalled Item: Bactroban Cream Recalled by GlaxoSmithKline, LLC Due to Penicillin Cross...

The Issue: Penicillin Cross Contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2016· J&D's Down Home Enterprises, Inc.

Recalled Item: Original Bacon Flavored Seasoning Salt Recalled by J&D's Down Home...

The Issue: Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Aribex Inc

Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...

The Issue: Firm received customer complaints where end users reported that Nomad Pro...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2016· Bovie Medical Corporation

Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...

The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...

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

Class II — Potential Health HazardOngoing