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 1286112880 of 49,744 recalls

Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...

The Issue: Due to a programmer software anomaly under very specific circumstance when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...

The Issue: Due to a programmer software anomaly under very specific circumstance when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· Becton Dickinson & Co.

Recalled Item: BD Synapsys Microbiology Informatics Solution Recalled by Becton Dickinson &...

The Issue: When updating BD Kiestra customers to BD Synapsys version 4.10, the custom...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· Roche Diabetes Care, Inc.

Recalled Item: RocheDiabetes Care Platform Software version 2.5.2 material number...

The Issue: Potential for patient data mismatch when using browser "back" button to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· Acumed LLC

Recalled Item: 4.0mm x 10mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...

The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· Acumed LLC

Recalled Item: 4.0mm x 12mm Cannulated Screw Recalled by Acumed LLC Due to Cannulated...

The Issue: Cannulated Screws 4.0mm x 10mm and 4.0mm x 12mm may not have sufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Standard PVC Laryngeal Masks Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The mask cuff may disconnect from the device's breathing tube.

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: Sermorelin Acetate Lyophilized powder for reconstitution Recalled by Olympia...

The Issue: Sub Potent

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: Hydroxocobalamin B12 1mg/mL Recalled by Olympia Compounding Pharmacy dba...

The Issue: Sub Potent

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: Sincalide Lyophilized powder for reconstitution Each ML contains: Mannitol...

The Issue: Super Potent and Failed Reconstitution Time

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: T-105 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to...

The Issue: Super Potent

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: Formula F9 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due...

The Issue: Sub Potent

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: SB-4 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to...

The Issue: Sub Potent

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

Class III — Low RiskOngoing
Refund
DrugMarch 8, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: NAD+ Nicotinamide Adenine Dinucleotide Recalled by Olympia Compounding...

The Issue: Product found to be Sub Potent or Exceeded reconstitution time

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2022· Fairmont Foods Inc.

Recalled Item: Schwan's Spinach & Artichoke Dip. Item Number 061353 Recalled by Fairmont...

The Issue: Cartons of Spinach Artichoke Dip may contain Chicken & Broccoli.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2022· Schreiber Foods Inc

Recalled Item: Shredded Cheese consisting of Monterey Jack Recalled by Schreiber Foods Inc...

The Issue: Potential to contain foreign material (metal).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2022· Olympus Corporation of the Americas

Recalled Item: BF-MP60: OES Bronchofiberscope Recalled by Olympus Corporation of the...

The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...

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

Class II — Potential Health HazardOngoing