Rigid Tip Suction Wand Non sterile bulk devices — Class II medical device recall Z-0650-2013
Terminated recall by California Medical Laboratories Inc, reported 2013-01-16, distributed in AZ, CA, CO, FL, LA, MS. California Medical Laboratories, Inc. has identified an issue with the Rigid Tip Suction Wand. Due to insuffic
| Recall number | Z-0650-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | California Medical Laboratories Inc, Costa Mesa, CA, United States |
| Recall initiated | 2012-11-02 |
| Classified | 2013-01-07 |
| Reported by FDA | 2013-01-16 |
| Terminated | 2013-03-04 |
| Distributed | AZ, CA, CO, FL, LA, MS |
| Countries outside the US | CA, ES, GR, HK, IE, IL, IN, JO, LB, MY, NL, RU, SA, ZA |
| Lot numbers | S112468N, S120196N, S120197N |
| Model numbers | SU-12202NS |
Product
Rigid Tip Suction Wand Non sterile bulk devices (S112468N, S120196N, and S120197N) were sold to Terumo UK to be included in a kit under Terumo as manufacturer's name. The Suction Wands are indicated for use to remove excess fluid from the surgical field.
Reason for recall
California Medical Laboratories, Inc. has identified an issue with the Rigid Tip Suction Wand. Due to insufficient adhesive application, the distal tip has the potential to come loose from the wand and fall into the patient's chest cavity.
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-0650-2013. 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.