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. 2,429 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,429 in last 12 months

Showing 3538135400 of 49,744 recalls

Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension EXL with LM STM Product Recalled...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· OrthoPediatrics Corp

Recalled Item: UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response...

The Issue: Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· C.R. Bard, Inc.

Recalled Item: Arctic Sun 5000 and Arctic Sun 2000 Recalled by C.R. Bard, Inc. Due to...

The Issue: Improper targeted temperature therapy was delivered to patients because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Zimmer, Inc.

Recalled Item: Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double...

The Issue: The firm identified a malfunction which made it possible for a handpiece to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2015· Siemens Healthcare Diagnostics Inc.

Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...

The Issue: Siemens has identified RMS compressors that are missing the safety cover on...

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

Class II — Potential Health HazardOngoing
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa 1 Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand and...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa Colostrum Capsules Recalled by Immuno - Dynamics, Inc Due to The...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: Colostrum Lozenges Recalled by Immuno - Dynamics, Inc Due to The PerCoBa...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: PerCoBa Whey Protein Isolate with Colostrum Recalled by Immuno - Dynamics,...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
FoodNovember 10, 2015· Immuno - Dynamics, Inc

Recalled Item: Colostrum Powder Recalled by Immuno - Dynamics, Inc Due to The PerCoBa brand...

The Issue: The PerCoBa brand and Synertek brand Colostrum product labels should state...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2015· Northwind Pharmaceuticals LLC

Recalled Item: Prednisone 20 mg Recalled by Northwind Pharmaceuticals LLC Due to Labeling:...

The Issue: Labeling: Not elsewhere classified. NDC number is incorrect on the container.

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2015· Freedom Pharmaceuticals Inc

Recalled Item: Baclofen USP powder Recalled by Freedom Pharmaceuticals Inc Due to Presence...

The Issue: Presence of Foreign Substance

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 9, 2015· C.R. Bard, Inc.

Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...

The Issue: The product may contain electronic components that lead to a premature...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2015· Medtronic Inc.

Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...

The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...

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

Class II — Potential Health HazardOngoing
FoodNovember 9, 2015· Nutritional Resources Inc

Recalled Item: Healthwise Recalled by Nutritional Resources Inc Due to Foreign matter...

The Issue: Foreign matter (plastic) was observed in the product.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 9, 2015· Zenobia Co.

Recalled Item: My Spice Sage Ground Flax Seed Meal under the following Recalled by Zenobia...

The Issue: Zenobia Company, LLC is recalling Flax Seed Meal due to the possible...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 8, 2015· Vidco, Inc.

Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...

The Issue: Testing at customer site showed unit Remote Patient Monitoring System...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2015· Remel Inc

Recalled Item: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10) Recalled...

The Issue: Antibiotic concentration may be insufficient which may result in incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2015· Myco Medical Supplies Inc

Recalled Item: Unolok Blunt Fill Needle 18G x 1.5" Red Recalled by Myco Medical Supplies...

The Issue: Particulates: Complaints of rubber coring from the closure of injection vials.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2015· Terumo Medical Corporation

Recalled Item: Destination Renal Guiding Sheath Intended for the introduction of...

The Issue: Based on internal investigation and testing that revealed the distal end of...

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

Class II — Potential Health HazardOngoing