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. 2,604 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
2,604 in last 12 months

Showing 1780117820 of 51,202 recalls

Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650600111 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #65220955 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650304917 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #650305414 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Medline Industries Inc

Recalled Item: Kit Model #65193091 Recalled by Medline Industries Inc Due to Non-sterile...

The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and...

The Issue: The device may detect an incorrect Heater Bag volume which may lead to a...

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

Class II — Potential Health HazardOngoing
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Panagel Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Genesis Hand Sanitizer Gel Recalled by Genesis Partnership Company SA Due to...

The Issue: CGMP Deviations: hand sanitizers were recalled because they were...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 11, 2020· Genesis Partnership Company SA

Recalled Item: Killz Germz Hand Sanitizer Recalled by Genesis Partnership Company SA Due to...

The Issue: Sub-Potent Drug; Killz GERMz was recalled due to sub-potent results. Testing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse PACS Software Versions 5.1 and higher Recalled by Fujifilm Medical...

The Issue: There is a potential for the wrong patient information may be displayed in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Bien-Air Surgery SN ******* MULTIFUNCTION PEDAL OSSEODUO - Recalled by...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Bien-Air Surgery SN ******* OSSEOSTAP Footcontrol - Product Recalled by...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse PACS Software Version 5.6.1 - Product Usage: intended for Recalled...

The Issue: FUJIFILM has become aware of the possibility that certain CT studies may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Bien-Air Surgery SN **** FOOTCTRL OSSEODOC - Product Recalled by Bien-Air...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Entellus Medical SN ******* Shaver System Foot Pedal Recalled by Bien-Air...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2020· Bien-Air Surgery Sa

Recalled Item: Stryker Instruments SN ******* S2 MINI FOOT Pedal Recalled by Bien-Air...

The Issue: The magnet located inside the foot pedal may come off and may result in...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2020· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical...

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
FoodSeptember 9, 2020· Gilster-Mary Lee Corp.

Recalled Item: Microwave popcorn packaged in the following ways: 1) Full Circle Recalled by...

The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...

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

Class II — Potential Health HazardOngoing
Refund