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Hillrom Temperature Management Controller, MP, Model #… recallZ-0841-2025 · Augustine Temperature Management, LLC · initiated Mar 14, 2022

Completed

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Augustine Temperature Management, LLC or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

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".

FDA root cause category: Device Design

What the company is doing

Augustine Temperature Management, LLC began correcting (installing ferrites and software updates) the affected devices February, 2022 and completed the actions in August 2023. The firm did not perform any notification to its consignees that corrections would be implemented.

Recall details

Recall number
Z-0841-2025
Status
Completed
Initiated by the company
Mar 14, 2022
Posted by the FDA
Jan 10, 2025
Recalling firm
Augustine Temperature Management, LLC
Quantity
77 units
Product code
DWJ
Distribution
Worldwide

Product description

Hillrom Temperature Management Controller, MP, Model # 2083516; used in conjunction with Warming Blankets and Mattresses.

Code information (models, lots, serial numbers)

Show the full code information (1k characters)

UDI-DI 00850011479582, Serial Numbers: 23010166, 23010167, 23010168, 23010169, 23010170, 23010171, 23010172, 23010173, 23010174, 23010175, 23010176, 23010177, 23010178, 23010179, 23010180, 23010181, 23010182, 23010183, 23010184, 23010185, 24020001, 24020002, 24020003, 24020004, 24020005, 24020006, 24030001, 24030002, 24030003, 24030004, 24030005, 24030021, 24030022, 24030023, 24030024, 24030025, 24030026, 24030027, 24030028, 24030029, 24030030, 24030016, 24030017, 24030018, 24030019, 24030020, 22120033, 24030011, 24030012, 24030013, 24030014, 24030015, 24030006, 24030007, 24030008, 24030009, 24030010, 24060001, 24060002, 24060003, 24060004, 24060005, 24060006, 24060007, 24060008, 24060009, 24060010, 24060024, 24060025, 24060026, 24060027, 24060028, 24060011, 24060012, 24060013, 24060014, 24060015.

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Other products in the same recall event

The FDA groups related products into one recall event (event 95913).

Sources and updates

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