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. 2,623 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,623 in last 12 months

Showing 72617280 of 49,744 recalls

DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: PHENYLephrine HCl 1000 mcg/10 mL in 0.9% Sodium Chloride Injection Recalled...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: fentaNYL 500 mcg/100 mL Recalled by SCA Pharmaceuticals, LLC Due to Lack of...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: VANCOMYCIN 1.25 g added to 0.9% Sodium Chloride 250 mL Injection Recalled by...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: HYDROmorphone HCl 30 mg/30mL in 0.9% Sodium Chloride Injection Recalled by...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: PHENYLephrine HCl 500 mcg/5 mL in 0.9% Sodium Chloride Injection Recalled by...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: SUCcinylcholine Chloride 200 mg/10mL Injection (Concentration = 20mg/mL)...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: PHENYLephrine HCl 500 mcg/5 mL in 0.9% Sodium Chloride Injection Recalled by...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: fentaNYL 2 Recalled by SCA Pharmaceuticals, LLC Due to Lack of Assurance of...

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
DrugNovember 9, 2023· SCA Pharmaceuticals, LLC

Recalled Item: fentaNYL 200 mcg/100 mL Recalled by SCA Pharmaceuticals, LLC Due to Lack of...

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
DrugNovember 9, 2023· Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop

Recalled Item: LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5%...

The Issue: Product Mix-up: Incorrect Product Formulation

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2023· Family Medical Supply Inc

Recalled Item: Oxygen Recalled by Family Medical Supply Inc Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2023· SUGARMDS LLC

Recalled Item: Dr. Ergin's SugarMD Recalled by SUGARMDS LLC Due to MARKETED WITHOUT AN...

The Issue: MARKETED WITHOUT AN APPROVED NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet PowerLED/HLED and PowerLED300 OR Light Systems Recalled by Getinge...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Blueline Series 30/80 OR Light Systems Recalled by Getinge Usa Sales...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Rolite OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Lucea - Lucea10/40 Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet PowerLEDII OR Light System Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Equipment OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Volista Recalled by Getinge Usa Sales Inc Due to A potential for a...

The Issue: A potential for a light system to fall in the operating room.

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

Class II — Potential Health HazardOngoing