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. 2,506 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,506 in last 12 months

Showing 2664126660 of 51,202 recalls

Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX PST03533 KIT APP STAPLER Product Usage: The Endo GIA Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm- 3.5mm(...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX LAPIMBGP1 ZESTAW DO MGBP (LAPIMBGP1) Product Usage: The Endo Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT00714 KIT SLEEVE Product Usage: The Endo GIA universal Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)LAPBARLECZNA ZESTAW BARIATRYCZNY LECZNA (2) KITBAR021- BARIATRIC KIT X1...

The Issue: Device may be missing a sled component. The sled component is responsible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2018· ConvaTec, Inc

Recalled Item: Convatec Esteem(TM) Synergy Stomahesive(R) Recalled by ConvaTec, Inc Due to...

The Issue: It was discovered that the stoma hole of one lots of the Esteem synergy...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Biocare Medical, LLC

Recalled Item: Vulcan Fast Red Chromogen Kit 2 Recalled by Biocare Medical, LLC Due to...

The Issue: Chromogen failed to develop due to a stability issue caused by environmental...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
FoodApril 24, 2018· Labrada Nutrition, Inc

Recalled Item: Lean Pro 8 Chocolate 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 24, 2018· Labrada Nutrition, Inc

Recalled Item: Lean Pro 8 Cookies & Cream 1 Recalled by Labrada Nutrition, Inc Due to...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 24, 2018· Labrada Nutrition, Inc

Recalled Item: Lean Pro 8 Vanilla 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Presence of Foreign Tablets/Capsules: One foreign tablet identified as...

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

Class II — Potential Health HazardOngoing
Refund