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. 2,411 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,411 in last 12 months

Showing 4140141420 of 49,744 recalls

Medical DeviceJune 23, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...

The Issue: Complaints of failed calibration.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...

The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2014· Novel Laboratories, Inc.

Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...

The Issue: Failed Impurity/Degradation Specification; 12-month stability time point

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

Class III — Low RiskOngoing
Refund
DrugJune 20, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; Out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 20, 2014· Stryker Endoscopy

Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...

The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· Laser Peripherals LLC

Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling

The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2014· ORIGIO, Inc

Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...

The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Diltiazem HCl Extended Release Capsules Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Mckesson Packaging Services

Recalled Item: Aspirin DR Enteric Coated Tablets Recalled by Mckesson Packaging Services...

The Issue: Failed Dissolution Specification; at the 12 month time interval.

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Pfizer Inc.

Recalled Item: Cardura XL (doxazosin mesylate extended release tablets Recalled by Pfizer...

The Issue: Failed Impurities/Degradation Specifications: Product from this lot may not...

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

Class III — Low RiskOngoing
Refund
DrugJune 19, 2014· Forest Pharmaceuticals Inc

Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...

The Issue: Failed Dissolution Specifications: Drug failed stage III dissolution testing.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 19, 2014· Country Life

Recalled Item: Country Life TARGET MINS CALCIUM MAGNESIUM With Vitamin D3 Complex Recalled...

The Issue: The affected lots do not meet quality standards due to insoluble particulates.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2014· Abbott Molecular

Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...

The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2014· Boston Scientific CRM Corp

Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...

The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2014· Hospira Inc.

Recalled Item: Marcaine (bupivacaine HCl) injection Recalled by Hospira Inc. Due to...

The Issue: Presence of Particulate Matter: Confirmed customer complaint of discolored...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen)...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Apri (desogestrel and ethinyl estradiol tablets USP) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
DrugJune 17, 2014· Teva Pharmaceuticals USA

Recalled Item: Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...

The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2014· Varian Medical Systems, Inc.

Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...

The Issue: Trend in reports of unexpected decrease in beam output in C-series High...

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

Class II — Potential Health HazardOngoing