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. 1,061 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,061 in last 12 months

Showing 15781–15800 of 51,202 recalls

Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Recalled by...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Vero Biotech, LLC

Recalled Item: GENOSYL DS Recalled by Vero Biotech, LLC Due to Reports received of NO...

The Issue: Reports received of NO measured below desired dose during transition between...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Recalled...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· Smith & Nephew, Inc.

Recalled Item: LEGION Posterior Stabilized OXINIUM Femoral Component Recalled by Smith &...

The Issue: The device components experienced a manufacturing process error that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2021· CooperVision Inc.

Recalled Item: CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable...

The Issue: Misaligned placement of an axis mark can cause the patient to experience...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: The ADVIA Chemistry XPT Chemistry System Recalled by Siemens Healthcare...

The Issue: ADVIA Chemistry System and Software Versions (V1.4 SMN 11314625 and V1.4...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2021· Stryker Spine

Recalled Item: Cortoss Bone Augmentation Material 5cc Cartridge Recalled by Stryker Spine...

The Issue: The products experienced a 12-hour excursion from the required temperature...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2021· Stryker Spine

Recalled Item: Cortoss Bone Augmentation Material 10cc Cartridge Recalled by Stryker Spine...

The Issue: The products experienced a 12-hour excursion from the required temperature...

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

Class II — Potential Health HazardOngoing
DrugMay 18, 2021· Miracle 8989

Recalled Item: PremierZEN Gold 7000 capsule Recalled by Miracle 8989 Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 18, 2021· Miracle 8989

Recalled Item: PremierZEN Platinum 8000 capsule Recalled by Miracle 8989 Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 18, 2021· Miracle 8989

Recalled Item: maXXzen Platinum 12000 capsule Recalled by Miracle 8989 Due to Marketed...

The Issue: Marketed without an approved NDA/ANDA - Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 17, 2021· Smiths Medical ASD Inc.

Recalled Item: JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G...

The Issue: Specific models and lot numbers of the Jelco Hypodermic Needle-Pro Fixed...

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

Class I — Serious Health HazardOngoing
FoodMay 15, 2021· Clio LLC

Recalled Item: Clio Yogurt Bar Raspberry / Peach Mini Club pack Clio Recalled by Clio LLC...

The Issue: Possible metal fragments in Yogurt Bars

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2021· Clio LLC

Recalled Item: Clio Vanilla / Strawberry Club pack Greek Yogurt Bars wrapped Recalled by...

The Issue: Possible metal fragments in Yogurt Bars

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2021· Clio LLC

Recalled Item: Clio Expresso Greek Yogurt Bars wrapped in a Chocolate Coating Recalled by...

The Issue: Possible metal fragments in Yogurt Bars

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 15, 2021· Clio LLC

Recalled Item: Clio Berry Acai flavored Less Sugar Yogurt Bar in a Recalled by Clio LLC Due...

The Issue: Possible metal fragments in Yogurt Bars

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

Class II — Potential Health HazardOngoing
Refund