FDA Device recall Z-0352-2017
Rigid Suction Canister 3000 CC and 2000 CC
- FDA Device
- Class II
- terminated
- Published 2016-11-09
On 2016-11-09 the FDA classified a Class II recall of Rigid Suction Canister 3000 CC and 2000 CC by Medline Industries, citing risk of implosion when the Rigid Suction Canister is subjected to excessive negative pressure during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0352-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-10 |
| Published | 2016-11-09 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medline Industries |
| Distribution | CA, CO, FL, GA, IL, MA, MD, MI, MO, NC, NE, NJ, NY, OH, OK, PA, TX, WA |
Product
Rigid Suction Canister 3000 CC and 2000 CC.
Reason
Risk of implosion when the Rigid Suction Canister is subjected to excessive negative pressure during use.
Identifiers
| code_info | RIGID CANISTER 2000 cc and 3000 cc with product code OR220 and OR230. Affected Lot Numbers 9961601xxxx through 9961604xxxx |
|---|
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-0352-2017%22
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