Data Foundry

Medical device recalls 2024

Custom procedural convenience kits and trays — Class II medical device recall Z-0823-2024

Ongoing recall by American Contract Systems, Inc., reported 2024-02-07, distributed nationwide. During an internal investigation, ACS identified that several components were "piggybacked" to ACS trays and s

Recall numberZ-0823-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAmerican Contract Systems, Inc., Temple Terrace, FL, United States
Recall initiated2023-11-29
Classified2024-01-26
Reported by FDA2024-02-07
DistributedNationwide (US)
Quantity1,031 units
UPC / GTIN / UDI-DI00191072117991, 00191072136688
Lot numbers643221, 651221, 701221, 727221, 751221, 769221, 846221, 912231, 938231, 939231, 973231
Expiration dates2023-06-03, 2023-09-06, 2023-10-26, 2023-12-15, 2023-12-23, 2024-01-27, 2024-03-02, 2024-03-03, 2024-03-29, 2024-08-19, 2024-09-30

Product

Custom procedural convenience kits and trays, urological, labeled as: a) UROLOGY DAVINCI PACK, kit number HGUR87G; b) CYSTO PACK, kit number LVCY20; c) URO ROBOTIC PACK, kit number LVUR44;

Reason for recall

During an internal investigation, ACS identified that several components were "piggybacked" to ACS trays and subjected to the ACS sterilization process. There is no supporting documentation stating the "piggybacked" components were assessed to determine if they were suitable for exposure to elevated temperatures for an extended period of time and further exposure to sterilization. As a result, the piggybacked components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) may have had higher than specified EO residuals.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0823-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.