Data Foundry

Medical device recalls 2015

Powered stretcher chair used during facial and eye surgeries — Class II medical device recall Z-0996-2015

Terminated recall by TransMotion Medical Inc, reported 2015-01-28. The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

Recall numberZ-0996-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmTransMotion Medical Inc, Sharon Center, OH, United States
Recall initiated2014-11-14
Classified2015-01-16
Reported by FDA2015-01-28
Terminated2015-07-11
Countries outside the USAU, CA, CL, CN, CR, DE, DZ, IL, IT, KR, MY, NG, NL, PL, PT, SA, SG, TH, VE
Quantity1,127 units
Serial numbers0212, 0303, 0304, 0306, 0321, 0329, 0330, 0332, 0333, 0346, 0347, 0348, 0349, 0350, 0357, 0358, 0359, 0360, 0361, 0362, 0363, 0371, 0372, 0374, 0377 and 475 more
Model numbersEHA14-21BKKJ-042, EHA34-23MKKJ-600, EHA35-23MKKJ-591, TM10-E, TM12, TM9, TM9-E, TMM5-100, TMM5-101, TMM5-102, TMM5-103, TMM5-104, TMM5-106, TMM5-114, TMM5-B, TMM5-EB, TMM5-TB, TMM5-TEB, TMM5-WB, TMM5-WTB, TMM5-WTEB, TMM5-XB, TMM5-XEB, TMM5-XFB, TMM5-XTB and 9 more

Product

Powered stretcher chair used during facial and eye surgeries. One chair per package.

Reason for recall

The firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0996-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.