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. 2,548 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,548 in last 12 months

Showing 1876118780 of 49,744 recalls

DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: rocuronium Bromide Recalled by PharMEDium Services, LLC Due to Firm is...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2020· Dr. Reddy's Laboratories, Inc.

Recalled Item: Phytonadione Injectable Emulsion Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Defective Container: Recall is due to breaking and shattering of ampules...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 16, 2020· Mountain Rose Inc. dba Mountain Rose Herbs

Recalled Item: Kudzu Root (Pueraria montana var. lobata) Recalled by Mountain Rose Inc. dba...

The Issue: Salmonella

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 16, 2020· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheter 6F Model 5540. For delivery of Recalled by...

The Issue: The inner lumen of the Langston catheter may separate from the hub during...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 16, 2020· Avanos Medical, Inc.

Recalled Item: CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit Recalled by Avanos...

The Issue: The CORFLO PEG tube may become blocked at the center of the adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test DNA Control-IVD for detection of DNA Recalled by...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test RNA/DNA Panel- IVD for detection of Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Ion Torrent Dx No Template Control Kit- IVD for detection Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2020· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test RNA Control- IVD for detection of Recalled by Life...

The Issue: Extended Expiration Date prior to clearance

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 13, 2020· Aesthetics Biomedical, Inc.

Recalled Item: SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Recalled by...

The Issue: A high frequency output (2 MHz) has not been cleared for distribution in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2020· Biomet, Inc.

Recalled Item: Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips...

The Issue: There were unknown bioburden levels prior to sterilization, which may affect...

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

Class II — Potential Health HazardOngoing
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Sprout Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Mixed Greens 4 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Spring Salad 6 oz. Product contains red clover sprouts. Recalled by Chicago...

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 12, 2020· Chicago Indoor Garden, Inc.

Recalled Item: Red Clover 4 oz Recalled by Chicago Indoor Garden, Inc. Due to Potential E....

The Issue: FDA sample analysis of sprouts was positive for E. coli. FDA traceback and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...

The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...

The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2020· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...

The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...

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

Class II — Potential Health HazardOngoing