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. 2,646 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,646 in last 12 months

Showing 1314113160 of 51,202 recalls

Medical DeviceMarch 11, 2022· Abbott Vascular

Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...

The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2022· Abbott Vascular

Recalled Item: INDEFLATOR Plus 30 - WPL2122277-01 (2019-03-01) Recalled by Abbott Vascular...

The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2022· Abbott Vascular

Recalled Item: 20/30 INDEFLATOR - WPL2122268-01 (2019-03-01) Recalled by Abbott Vascular...

The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2022· Abbott Vascular

Recalled Item: 20/30 Priority Pack Accessory Kit/.096 RHV - WPL2122270-01 Recalled by...

The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2022· Abbott Vascular

Recalled Item: 20/30 Priority Pack w/COPILOT - WPL2122272-01 (2019-03-01) Recalled by...

The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...

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

Class II — Potential Health HazardOngoing
DrugMarch 10, 2022· Macleods Pharma Usa Inc

Recalled Item: Risedronate Sodium Tablets Recalled by Macleods Pharma Usa Inc Due to FAILED...

The Issue: FAILED CONTENT UNIFORMITY SPECIFICATIONS

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

Class III — Low RiskOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 721-1000 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 744-4930 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 714-5000 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 721-0200 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 722-0105 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 714-0706 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 731-0120 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 744-4875 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Continental Mills (Corporate Office)

Recalled Item: Item # 743-0278 Recalled by Continental Mills (Corporate Office) Due to...

The Issue: foreign materials

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2022· Sauer Brands Inc - New Century

Recalled Item: Caesar dressing in a 1.5 oz pouch Recalled by Sauer Brands Inc - New Century...

The Issue: Undeclared Allergen - Soy

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...

The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...

The Issue: Due to a programmer software anomaly under very specific circumstance when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...

The Issue: Due to a programmer software anomaly under very specific circumstance when...

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

Class II — Potential Health HazardOngoing