Reported Feb 7, 2024 · Ongoing

Custom procedural convenience kits and trays, general hospital use, labeled as

American Contract Systems, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: American Contract Systems, Inc. · 7802 E Telecom Pkwy · Temple Terrace, FL · 33637-0928

Is this the product you have?

Custom procedural convenience kits and trays, general hospital use, labeled as

4 of 4 products

Products covered by this recall
#Product as published
1Baby PICC Kit, kit number UIBP90J
2Baby PICC Kit, kit number UIBP90K
3PORT PACK (PS 058330), kit number UIPO82AB
4Pediatric PICC Kit, kit number UIPP76K
Lot codes and dates

4 of 4 products

Products covered by this recall
#BarcodesProduct as published
100191072117038UIBP90J, UDI/DI 00191072117038, Lot Numbers: 996231, exp. 1/4/2024
200191072189356UIBP90K, UDI/DI 00191072189356, Lot Numbers: 911231, exp. 7/26/2023
300191072172006UIPO82AB, UDI/DI 00191072172006, Lot Numbers: 727221, exp. 9/30/2023; 680221, exp. 11/16/2023
400191072142849UIPP76K, UDI/DI 00191072142849, Lot Numbers: 637221, exp. 12/29/2023; 976231, exp. 1/24/2024; 898231, exp. 4/12/2024
Amount recalled
244 units

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:19 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.