FDA Device recall Z-0120-2019
Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer
- FDA Device
- Class II
- terminated
- Published 2018-10-24
On 2018-10-24 the FDA classified a Class II recall of Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer by A M Systems, citing some of the Disposable Smooth Interior Tubing may pull apart when stretched.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0120-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-08-10 |
| Published | 2018-10-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | A M Systems |
| Distribution | NC, OH, PA |
Product
Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer. This tubing is supplied non-sterile P/N: 1024920 Rev. 01 Low temperature smooth interior tubing is a disposable pulmonary equipment interconnect used in ventilation and aesthesia machines.
Reason
Some of the Disposable Smooth Interior Tubing may pull apart when stretched.
Identifiers
| code_info | Product Code: 243301 Lot Numbers: 572015 574717 578973 579100 582567 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0120-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.