Class II — J&J Solutions, Inc. DBA Corvida Medical
| Recalling firm | W+S Solutions GmbH |
|---|---|
| Registered facility | W+S SOLUTIONS GMBH (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Product malfunction: Needle does not retract. |
| Product | Halo Closed System Transfer Device, closed syringe adaptor, REF CSA100, Rx only, Sterile, packaged as individual units, packed and shipped 60 units/box and 4 boxes/shipping carton Corvida Medical, Coralville, IA 52241. |
| Quantity | 5520 units |
| Distribution | US Distribution to the states of : MD, TX, and WI. There was no foreign/military/government distribution. |
| Initiated | 2016-11-22 |
| Classified | 2017-01-11 |
| Terminated | 2018-11-09 |
| Recall number | Z-1003-2017 |
| 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 — J&J Solutions, Inc. DBA Corvida Medical (Z-1003-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/75810/
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