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. 1,055 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
1,055 in last 12 months

Showing 16501–16520 of 49,744 recalls

Medical DeviceJanuary 4, 2021· Aomori Olympus Co., Ltd.

Recalled Item: NA-201SX-4021 ASPIRATION NEEDLE VIZISHOT 21G Recalled by Aomori Olympus Co.,...

The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2021· Ethicon, Inc.

Recalled Item: Ethicon Dermabond Advanced Topical Skin Adhesive-topical skin adhesive to...

The Issue: Product distributed with a red tape as part of the sterile packaging which...

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

Class II — Potential Health HazardOngoing
FoodJanuary 4, 2021· Ittella International, LLC

Recalled Item: Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life...

The Issue: A gluten free claim was inadvertently used on the lid of the container....

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 4, 2021· Nostrum Laboratories Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...

The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 1, 2021· Precision Dose Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse USP 0.12% Recalled by Precision Dose Inc....

The Issue: cGMP deviations: The firm was notified of the manufacturer's expanded recall.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· AuroMedics Pharma LLC

Recalled Item: Acetaminophen Injection 1 Recalled by AuroMedics Pharma LLC Due to...

The Issue: Discoloration and failed pH specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2020· Allergan, PLC.

Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...

The Issue: Labeling: Missing instructions for use insert

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 30, 2020· Beckman Coulter Inc.

Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...

The Issue: The Quality Control (QC) card has a label error for the standard deviation...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2020· Mar-Med Co

Recalled Item: Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if...

The Issue: A failure can occur if the user attempts to remove the device by partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2020· Baxter Healthcare Corporation

Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...

The Issue: Potential for the battery to lose its ability to be recharged.

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

Class II — Potential Health HazardOngoing
DrugDecember 28, 2020· Sunstar Americas, Inc.

Recalled Item: Paroex (Chlorhexidine Gluconate) Oral Rinse Recalled by Sunstar Americas,...

The Issue: cGMP Deviations; FDA inspection of manufacturing facility observed potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 28, 2020· Akorn, Inc.

Recalled Item: Levetiracetam Oral Solution Recalled by Akorn, Inc. Due to Defective...

The Issue: Defective container: Customer complaints for oral solution leaking from bottles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 24, 2020· Philips Ultrasound Inc

Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...

The Issue: Control panel arm assembly could have missing or loose screws where undue...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2020· Philips North America

Recalled Item: PHILIPS Incisive Computed tomography X-ray system Incisive CT Software...

The Issue: Patient tabletop moved out to the home position during scan initialization,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2020· Draegar Medical Systems, Inc.

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

The Issue: The Infinity M540 patient monitor may randomly reboot due to an error to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2020· Biomet, Inc.

Recalled Item: A.L.P.S. Clavicle Plating System Recalled by Biomet, Inc. Due to The...

The Issue: The instruments may become cold welded together when the drill is inserted...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Valkyrie LTOWB Collection (P/N 80-820 Recalled by Combat Medical Systems,...

The Issue: There is the potential of a bent or disconnected needle in one of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Recalled by...

The Issue: There is the potential of a bent or disconnected needle in one of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN Recalled by Combat...

The Issue: There is the potential of a bent or disconnected needle in one of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 23, 2020· Combat Medical Systems, LLC

Recalled Item: Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Recalled...

The Issue: There is the potential of a bent or disconnected needle in one of the...

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

Class I — Serious Health HazardOngoing