Rigid Suction Canister 3000 CC and 2000 CC — Class II medical device recall Z-0352-2017
Terminated recall by Medline Industries Inc, reported 2016-11-09, distributed in CA, CO, FL, GA, IL, MA, MD, MI…. Risk of implosion when the Rigid Suction Canister is subjected to excessive negative pressure during use.
| Recall number | Z-0352-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Mundelein, IL, United States |
| Recall initiated | 2016-08-10 |
| Classified | 2016-11-03 |
| Reported by FDA | 2016-11-09 |
| Terminated | 2019-06-03 |
| Distributed | CA, CO, FL, GA, IL, MA, MD, MI, MO, NC, NE, NJ, NY, OH, OK, PA, TX, WA |
| Quantity | 7,680 units |
| Lot numbers | 9961601XXXX |
Product
Rigid Suction Canister 3000 CC and 2000 CC.
Reason for recall
Risk of implosion when the Rigid Suction Canister is subjected to excessive negative pressure during use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0352-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.