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. 2,394 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,394 in last 12 months

Showing 4302143040 of 49,744 recalls

FoodJanuary 29, 2014· Gano Excel USA Inc

Recalled Item: Gano C'Real Spirulina Recalled by Gano Excel USA Inc Due to Undeclared Wheat

The Issue: Gano Excel USA is recalling the C'Real Spirulina because it contains...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2014· Implantech Associates Inc

Recalled Item: Gelzone Shoulder Sleeve Recalled by Implantech Associates Inc Due to...

The Issue: Implantech initiated the voluntary recall of Gelzone Shoulder Sleever,...

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

Class II — Potential Health HazardOngoing
DrugJanuary 28, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Carisoprodol Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurity/degradation Specification

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

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by Caraco Pharmaceutical...

The Issue: Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 28, 2014· AlterG, Incorporated

Recalled Item: Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the...

The Issue: Unapproved material used by vendor in subset of shorts causing them to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2014· AMO Puerto Rico Manufacturing, Inc.

Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...

The Issue: Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.

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

Class II — Potential Health HazardOngoing
DrugJanuary 27, 2014· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product did not meet...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2014· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product did not meet...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 27, 2014· Kellogg Company

Recalled Item: Pringles Recalled by Kellogg Company Due to Undeclared Milk

The Issue: Undeclared milk, an allergen

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Dynamics Picture Archiving and Communication System (PACS). Model...

The Issue: Potential patient data mixup. Improper error handling could allow for two...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2014· Synthes, Inc.

Recalled Item: Synthes Small Notch Titanium Reconstructive Plate Product Usage: The Synthes...

The Issue: Certain modules containing the Synthes Small Notch Titanium Reconstructive...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2014· Cardiovascular Systems, Inc.

Recalled Item: CSI Recalled by Cardiovascular Systems, Inc. Due to Cardio vascular Systems...

The Issue: Cardio vascular Systems Inc. has initiated a recall to request the immediate...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 27, 2014· Synthes, Inc.

Recalled Item: Synthes 3.2 mm Guide Wire 400mm. Used for guiding the Recalled by Synthes,...

The Issue: Synthes 3.2 mm Guide Wire 400mm included an incorrect raw material listed on...

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

Class II — Potential Health HazardOngoing
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Fruta BIO 400 mg capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Meizitang Strong Version Botanical Slimming Recalled by MyNicNaxs, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Meizi Evolution Soft Gel Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Pill for weight reduction Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: SlimEasy Herbs Capsule Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: JIANFEIJINDAN Activity Girl Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Super Fat Burning Bomb Capsules Recalled by MyNicNaxs, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund