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. 2,502 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,502 in last 12 months

Showing 2040120420 of 49,744 recalls

DrugSeptember 17, 2019· Akorn, Inc.

Recalled Item: Lidocaine Hydroclhoride Jelly USP Recalled by Akorn, Inc. Due to cGMP...

The Issue: cGMP Deviations: firm reported finding metal particulate matter in the...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 17, 2019· SOUTHEASTERN GROCERS - MARKETI

Recalled Item: SE Grocers **BAKERY** 18 CT Variety Pack Cookies Recalled by SOUTHEASTERN...

The Issue: 18 count Variety Pack cookies made in-store bakeries included Peanut Butter...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 17, 2019· SOUTHEASTERN GROCERS - MARKETI

Recalled Item: SE Grocers **BAKERY** 18 CT Peanut Butter Cookies Recalled by SOUTHEASTERN...

The Issue: 18 count Peanut Butter cookies made in-store bakeries failed to declare...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2019· Cook Inc.

Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...

The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Icecure Medical Ltd

Recalled Item: IceCure Cryoablation System ProSense -Intended for cryogenic destruction of...

The Issue: Updated User Manual DSR3200000 Rev. E to include the safety guidelines in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· KT Health, LLC

Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...

The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· GE Healthcare, LLC

Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...

The Issue: Potential for failure of the patient leakage current test. There is a...

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

Class II — Potential Health HazardOngoing
DrugSeptember 13, 2019· GUERBET LLC

Recalled Item: Sodium Chloride Injection USP 0.9% Recalled by GUERBET LLC Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 13, 2019· GUERBET LLC

Recalled Item: Optiray 320 (ioversol) Injection 68% Recalled by GUERBET LLC Due to...

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 13, 2019· Abbott Laboratories

Recalled Item: Abbott Calcilo XD Recalled by Abbott Laboratories Due to Off color and odor....

The Issue: Off color and odor. Compromised can seam due to product (powder) in the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 13, 2019· Draegar Medical Systems, Inc.

Recalled Item: The Infinity Acute Care System (IACS) Monitoring Solution with the Recalled...

The Issue: Cybersecurity vulnerabilities may cause device to reboot, lose alarm...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Recalled by KRS Global Biotechnology, Inc 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