Medical Device Recall: Z-0031-2025

FDA Recalls dataset · Firm: Windstone Medical Packaging, Inc. · Status: Open, Classified

Recall Action Class: N/A Date Initiated: 2024-08-16 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0031-2025.

Recall Res Number
Z-0031-2025
Recalling Firm / Manufacturer
Windstone Medical Packaging, Inc.
FEI Number
1000125955
Recall Status
Open, Classified
Recall Classification
N/A
Date Initiated
2024-08-16
Date Posted
2024-10-08
Date Terminated
N/A
Product Code
LRO
Event Number
95306
Product Quantity
180 packs
Product Description Aligned Medical Tonsil Pack REF AMS14809 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Reason for Recall Due to convenience kits containing a kit component that is under a recall action for improper use.
Action Details On 08/16/2024, the firm email an "URGENT: MEDICAL DEVICE PRODUCT CORRECTION" Letter to customers informing them that Cardinal Health is conducting a product correction for its Salem Sump PVC Tubes. These Sump PVC tubes were included in the Aligned Medical convenience kits. The correction for this Recall is an updated product label, an electronic instruction for use (eIFU). The updated labeling is to address improper use of the Sump PVC tubes which can lead to breakage of the Salem Sump Anti Reflux Valve (ARV) that increases risk to patients. Customers are instructed to: 1. Review your inventory for the affected kits, all lots are impacted 2. Communicate the change to the use instructions with all personnel that utilize Salem Sump" products contained within AMS kits. 3. If you have further distributed this product, please identify your distribution partners, and notify them at once of the product correction. Your notification to your customers should include a copy of this notification letter. 4. Please complete and return the AMS Urgent Medical Device Product Correction Response Required form within 5 business days and return via email to fieldcorrectiveaction@alignedmedical.com even if you have no affected product on hand. For questions or concerns, contact Aligned Medical Solutions at fieldcorrectiveaction@alignedmedicalsolutions.com
Distribution Pattern U.S. Nationwide distribution in the states of CA, MO, OH, VA, and WY.
Code Information / Serial Numbers Catalog Number: AMS14809 UDI-DI code: B098AMS148090 Lot Numbers: 192737 194922 200224 200950 203412

Related Establishments / Registrations

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