FDA Device recall Z-0435-2014
VersaSafe Extension Set, Model No. 21000M-007
- FDA Device
- Class II
- terminated
- Published 2013-12-11
On 2013-12-11 the FDA classified a Class II recall of VersaSafe Extension Set, Model No. 21000M-007 by Carefusion 303, citing careFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as inten….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0435-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-08 |
| Published | 2013-12-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
VersaSafe Extension Set, Model No. 21000M-007
Reason
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
Identifiers
| code_info | Lot No. 13066550 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Other recalls by Carefusion 303
- BD Pyxis MedStation ES Tower REF: 352 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis Anesthesia Station ES REF: 327 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis MedBank Mini REF: 1147-00 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303 - BD Pyxis Anesthesia Station 4000 REF: 338 Medication cabinet
FDA Device · Class II · 2026-06-10 · Carefusion 303
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0435-2014%22
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