Product Recalls in Louisiana

Product recalls affecting Louisiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Louisiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,469 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,469 in last 12 months

Showing 4042140440 of 51,202 recalls

DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodFebruary 27, 2015· Unilever United States, Inc.

Recalled Item: Talenti Gelato & Sorbetto Recalled by Unilever United States, Inc. Due to...

The Issue: Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Stryker received four customer complaints reporting that inside the box...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 26, 2015· Ethicon Endo-Surgery Inc

Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...

The Issue: During an internal inspection of the production process the firm discovered...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...

The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Quest Medical, Inc.

Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...

The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2015· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...

The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2015· Heritage Pharmaceuticals, Inc.

Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2015· Amerx Health Care Corp.

Recalled Item: Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp....

The Issue: Nonapproved labeling claims (Sterile)

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific: Expel" Drainage Catheter with Twist-Loc" Hub APDL...

The Issue: Boston Scientific is initiating this Medical Device Field Correction of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2015· Biosense Webster, Inc.

Recalled Item: LASSO NAV Duo Loop eco Catheters Recalled by Biosense Webster, Inc. Due to...

The Issue: Biosense Webster is recalling the LASSO NAV Duo Loop eco Catheters because...

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

Class II — Potential Health HazardOngoing
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund