FDA Device recall Z-0842-2025
Augustine Surgical Inc
- FDA Device
- Class II
- completed
- Published 2025-01-22
On 2025-01-22 the FDA classified a Class II recall of Augustine Surgical Inc by Augustine Temperature Management, citing hotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0842-2025 |
| Classification | Class II |
| Status | completed |
| Initiated | 2022-03-14 |
| Published | 2025-01-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Augustine Temperature Management |
| Distribution | n/a |
Product
Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Single Port, Models: 1) WC71V; 2) WC71V-DEMO; 3) WC71V-R; used in conjunction with Warming Blankets and Mattresses, veterinary use.
Reason
HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 may experience a Power-on self-test error code "EA POST".
Identifiers
| code_info | 1) UDI/DI 00850011479247, Serial Numbers: 20090015, 20090016, 20090017, 20090018, 20090020, 20090021, 20090022, 200900…1) UDI/DI 00850011479247, Serial Numbers: 20090015, 20090016, 20090017, 20090018, 20090020, 20090021, 20090022, 20090023, 20090024, 20090025, 20090026, 20090027, 20090028, 20090029, 20090030, 20090031, 20090032, 20090033, 20090034, 20090035, 20090036, 20090037, 20090038, 20090039, 20090040, 20090041, 20090042, 20090043, 20090044, 20100030, 20100031, 20100032, 20100033, 20100034, 20100035, 20100036, 20100037, 20100038, 20100040, 20100041, 20100042, 20100043, 20100044, 20100045, 20100046, 20100047, 20100048, 20100049, 20100050, 20100051, 20100052, 20100053, 20100054, 20100055, 20100056, 20100057, 20100058, 20100059, 20100091, 20100092, 20100093, 20100094, 20100095, 20100096, 20100097, 20100098, 20100099, 20100100, 20100101, 20100103, 20110000, 20110001, 20110002, 20110003, 20110004, 20110005, 20110006, 20110006, 20110007, 20110008, 20110009, 20110010, 20110011, 20110012, 20110013, 20110014, 20110015, 20110016, 20110017, 20110018, 20110019, 20110020, 20110021, 20110022, 20110023, 2011002 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0842-2025%22
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