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. 1,041 recalls have been distributed to Louisiana in the last 12 months.

51,202 total recalls
1,041 in last 12 months

Showing 17181–17200 of 51,202 recalls

Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...

The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18cm) APPX 0.43ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 60" (152 cm) Appx 1.9 ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 154 cm (61 IN) APPX 1.5ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· ICU Medical, Inc.

Recalled Item: 60 IN (152cm) APPX 1.5 ml Recalled by ICU Medical, Inc. Due to Due to the...

The Issue: Due to the incorrect filter assembly.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Medela AG Medical Technology

Recalled Item: Stryker Medela .0193 AXS Universal Aspiration Tubing (01)07612367053921 -...

The Issue: Incorrect expiration date of "2023-07-24" on label of sterile tubing....

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2020· Flowers Foods (Corporate Offices)

Recalled Item: CANYON BAKEHOUSE GLUTEN MOUNTAIN WHITE BREAD NET WT. 18oz (1lb Recalled by...

The Issue: The firm discovered that some of their products showed higher than...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2020· Flowers Foods (Corporate Offices)

Recalled Item: CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ Recalled by...

The Issue: The firm discovered that some of their products showed higher than...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm x10mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 20mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Biomet, Inc.

Recalled Item: Vanguard 360 Revision System Posterior Augment With Bolt - Product Recalled...

The Issue: Incorrect bolt -tibial bolts in package instead of femoral bolts may delay...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm Recalled...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2020· Boston Scientific Corporation

Recalled Item: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm...

The Issue: The rotating luer fitting at the distal end of the delivery system handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Recalled by Siemens Medical...

The Issue: When the user changes frame rates from lower frequency (e.g. 10 f/s) to...

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2020· US Compounding Inc

Recalled Item: Neostigmine Methylsulfate PF Inj. 5 mg/5 mL Recalled by US Compounding Inc...

The Issue: Labelling: Missing label.

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2020· Torrent Pharma Inc

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC BIPOLAR Hip System Bi Polar Locking Ring Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing