FDA Device recall Z-0969-2013
Sterile Access & Return Line Set, 36" Length, Part # UM-872-36
- FDA Device
- Class II
- terminated
- Published 2013-03-27
On 2013-03-27 the FDA classified a Class II recall of Sterile Access & Return Line Set, 36" Length, Part # UM-872-36 by Molded Products, citing the recalled product leaks at the connection site.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0969-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-19 |
| Published | 2013-03-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Molded Products |
| Distribution | MI |
Product
Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically prescribed hemodialysis blood tubing.
Reason
The recalled product leaks at the connection site.
Identifiers
| code_info | Lot numbers: 80106 and 80106b |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0969-2013%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.