FDA Device recall Z-0174-2020
Semi-Rigid Suction Canister, 3000cc
- FDA Device
- Class II
- ongoing
- Published 2019-10-30
On 2019-10-30 the FDA classified a Class II recall of Semi-Rigid Suction Canister, 3000cc by Medline Industries, citing potential for the Semi-Rigid canister lid to fragment during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0174-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-01-31 |
| Published | 2019-10-30 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two boxes. One box includes 50 eaches of liners in a poly bag and the second box includes 50 eaches of lids in a poly bag. For OR530H, the customer receives the number of liners and lids purchased in one case without the individual boxes. The "H" denotes a single quantity when being ordered.
Reason
Potential for the Semi-Rigid canister lid to fragment during use.
Identifiers
| code_info | Model Numbers OR530, OR530H; Lot Numbers 20180914-1, 20180913-1, 20180916-1, 20180929-1 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0174-2020%22
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