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.
Showing 26861–26880 of 29,201 recalls
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure Nephrostomy Balloon Catheter. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Elekta digital accelerators with electrons and beam modulator Recalled...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Service Replacement 0-Ring. Used in as a service part Recalled by...
The Issue: Incorrect rubber nitrile O-rings distributed instead of the correct material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMICUS Exchange Kit Recalled by Fenwal Inc Due to Fenwal has initiated a...
The Issue: Fenwal has initiated a voluntary Urgent Product Recall for lot FA12C07070 of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Medical Collection Bag Recalled by International Biomedical, Ltd. Due to...
The Issue: International Biomedical has received reports of interference between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is Recalled...
The Issue: The outer sleeve would not fit over the S-LIFT Inserter assembly because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYRUS ACMI Recalled by Gyrus Acmi, Incorporated Due to lack of sterility...
The Issue: lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-720-000S5 T5 Pullover Toga w/Peel Away Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile...
The Issue: This is a recall expansion from the 2010 recall which now includes seven...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-820-000 T4 Zipper Toga (L/XL) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-850-100 T5 zipper Toga with Peel Away Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-760-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Hammock Mesh Sling (Junior) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments0400-720-000 T4 Pullover Toga (L/XL) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BC Hammock Mesh Sling (Large) Recalled by Prism Medical Services USA Due to...
The Issue: The product does not meet the firm's size standards, the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-820-100 T5 Zipper Toga with Peel Away Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-710-000 T4 Pullover Toga (S/M) Sterile Recalled by...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Instruments 0400-830-000 T4 Toga Recalled by Stryker Instruments...
The Issue: Based on an accelerated aging test for this product packaging, there is an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.