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. 2,489 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,489 in last 12 months

Showing 2156121580 of 49,744 recalls

DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: ROPIVICAINE 0.2% Recalled by RXQ Compounding 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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV) Recalled by RXQ...

The Issue: Crystallization

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: MAGNESIUM 200 MG/ML/ CALCIUM GLUC 6MG/ML/ ZINC 1MG/ML Recalled by RXQ...

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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: CYANCOBALAMIN 1200MCG/ML MDV INJECTION Recalled by RXQ Compounding LLC Due...

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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: PHENYLEPHRINE HCL 100 MCG/ML IN NACL 0.9% SYR Recalled by RXQ Compounding...

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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: GLUTATHIONE 200MG/ML (PFV) INJECTION SOLN Recalled by RXQ Compounding LLC...

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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: ONDANSETRON 2 MG/ML INJECTION SOLUTION (NPF) Recalled by RXQ Compounding LLC...

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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: NEOSTIGMINE METHYL SULFATE 1MG/ML INJ SOL SYR Recalled by RXQ Compounding...

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
DrugJune 19, 2019· RXQ Compounding LLC

Recalled Item: EDETATE CALCIUM DISODIUM 150MG/ML INJECTABLE Recalled by RXQ Compounding LLC...

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
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 3" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Elekta, Inc.

Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...

The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-25 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage:...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing