Class II — Cardinal Health 200, LLC
| Recalling firm | Cardinal Health 200, LLC |
|---|---|
| Registered facility | View this company's 35 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Completed |
| Reason | Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product |
| Product | Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011 |
| Quantity | N/A |
| Distribution | Nationwide Foreign: AU, BE, CA, DK, FI, GB, IE, NL |
| Initiated | 2019-04-30 |
| Classified | 2019-07-23 |
| Recall number | Z-2036-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Cardinal Health 200, LLC (Z-2036-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82927/
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