FDA Device recall Z-0772-2018
V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)
- FDA Device
- Class II
- terminated
- Published 2018-03-07
On 2018-03-07 the FDA classified a Class II recall of V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) by Steris, citing correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0772-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-09-28 |
| Published | 2018-03-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Steris |
| Distribution | AK, AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000)
Reason
Correction to update sterilizer software to prohibit the use of expired sterilant prior to the start of a sterilization cycle.
Identifiers
| code_info | Serial numbers: 031591505 031611402 032941412 031831609 030261761 033161412 030991616 032641604 03145…Serial numbers: 031591505 031611402 032941412 031831609 030261761 033161412 030991616 032641604 031451507 031621401 031691412 032941414 032861406 032941415 033141452 032861409 033161411 030231501 033241412 033241413 033241414 030231504 030231505 030231507 030231509 030231502 033151407 030341528 030441516 030231506 030231508 030341524 030341535 030361549 030361550 030501523 030501524 030501525 030681530 030681532 030341527 030681531 030341532 030341530 030441517 030341533 030441518 032861410 030341529 030501526 032941413 031191508 033181425 030341526 030441519 030441520 030501528 031191511 031271517 031191509 031191510 031341503 031341504 031271520 031271524 031351514 031451508 031351510 031351515 031411503 030341534 031411501 031411502 031451511 031451512 031271518 031591501 031591502 031591509 031591510 031591512 030361552 031451506 031541506 031451503 031541501 031541502 031541505 031541507 031541504 031591503 031591504 030681534 031351513 031591513 031631513 031631 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0772-2018%22
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