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. 1,105 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
1,105 in last 12 months

Showing 9721–9740 of 49,744 recalls

Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan 0-Deg Scrotal 20 Cm Recalled by Coloplast Manufacturing US, LLC Due to XXX

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Covidien, LP

Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...

The Issue: Medtronic was made aware of a supplier calibration issue during the contract...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch Scro Zero Ang 20cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch Scro Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch NB Scrot Zero 18cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan NB Scrotal Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Pump Assembly Recalled by Coloplast Manufacturing US, LLC Due to A...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Terumo Cardiovascular Systems Corporation

Recalled Item: CAPIOX NX19 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...

The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan 0-Deg Scrotal 18 Cm Recalled by Coloplast Manufacturing US, LLC Due to...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan NB Infra Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC Due...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan 0-Deg Infrapubic 20 Cm Recalled by Coloplast Manufacturing US, LLC Due...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch NB Infr Zero 16cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...

The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Elekta Inc

Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...

The Issue: Re-optimization, after adding contours without forced density outside the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Omega Medical Imaging, Inc.

Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...

The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...

The Issue: The external diameter of the biopsy instrument is larger than the internal...

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

Class II — Potential Health HazardOngoing
FoodFebruary 28, 2023· Russell Stover Candies Inc

Recalled Item: Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag...

The Issue: Outer package is mislabeled and does not declare tree nuts (pecans).

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2023· Sagent Pharmaceuticals Inc

Recalled Item: Heparin Sodium Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Labeling: Not elsewhere classified

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2023· FUJIFILM Healthcare Americas Corporation

Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...

The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...

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

Class II — Potential Health HazardOngoing