STERRAD 200 System Carriage — Class II medical device recall Z-0998-2013
Terminated recall by Advanced Sterilization Products, reported 2013-04-03, distributed nationwide. Advanced Sterilization Products (ASP) is recalling the STERRAD 200 System Carriage because it can potentially
| Recall number | Z-0998-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Sterilization Products, Irvine, CA, United States |
| Recall initiated | 2012-03-13 |
| Classified | 2013-03-26 |
| Reported by FDA | 2013-04-03 |
| Terminated | 2014-05-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CN, CZ, DE, EG, FR, GB, GR, HK, HU, IE, IL, IT, JP, KR, PL, SA, SE, SG, TH, TW |
| Quantity | 2,457 units |
Product
STERRAD 200 System Carriage, P/N 10208. Used as a tool to expedite loading and unloading processed items from a STERRAD 200 sterilizer.
Reason for recall
Advanced Sterilization Products (ASP) is recalling the STERRAD 200 System Carriage because it can potentially become dislodged when an excessive load is applied.
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-0998-2013. 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.