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. 2,591 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,591 in last 12 months

Showing 1818118200 of 51,202 recalls

Medical DeviceJuly 30, 2020· Cardinal Health 200, LLC

Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...

The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 10 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 2 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Undeclared Benzyl

The Issue: Cross Contamination with Other Product(s): containers labeled as having...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 29, 2020· SCA Pharmaceuticals

Recalled Item: Heparin Sodium 5 Recalled by SCA Pharmaceuticals Due to Subpotent Drug:...

The Issue: Subpotent Drug: Out-of-Specification potency results at the 30-day stability...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Avanos Medical, Inc.

Recalled Item: AVANOS MIC-KEY SF Gastrostomy Feeding Tube Recalled by Avanos Medical, Inc....

The Issue: Devices had cracked or detached from the feeding tube body

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 5.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Cardinal Health 200, LLC

Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: Recalled by...

The Issue: A degradation defect was found that could lead to holes and donning tears at...

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

Class II — Potential Health HazardOngoing