RecallRadar

FDA Device recall Z-0996-2015

Powered stretcher chair used during facial and eye surgeries

On 2015-01-28 the FDA classified a Class II recall of Powered stretcher chair used during facial and eye surgeries by Transmotion Medical, citing the firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0996-2015
ClassificationClass II
Statusterminated
Initiated2014-11-14
Published2015-01-28
Last updated2026-09-13 11:53 UTC
CompanyTransmotion Medical
Distributionn/a

Product

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

Reason

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

Identifiers

code_info
TMM supplier model numbers: EHA34-23MKKJ-600 EHA14-21BKKJ-042 EHA35-23MKKJ-591 The following Model numbers and Se…TMM supplier model numbers: EHA34-23MKKJ-600 EHA14-21BKKJ-042 EHA35-23MKKJ-591 The following Model numbers and Serial numbers are included in this recall: Model Number: TM10-E Serial number: 4678 Model Number: TM12 Serial numbers: 3362 3468 3810 4335 4336 4626 5068 5069 Model Number: TM9 Serial numbers: 2335 2337 2338 2679 2701 2785 2786 2787 2788 2789 2931 2981 2982 2983 3025 3398 3470 3471 3472 3473 3477 3478 3793 3794 4274 4275 4301 4302 4303 4304 4305 4306 4307 4755 4756 4757 4758 4759 4760 4761 Model Number: TM9-E Serial numbers: 3537 3750 3751 3752 4113 4425 4426 4427 4428 4429 4430 4431 4432 4433 4434 4435 4436 4437 4561 4562 4790 4791 4792 4793 4794 4795 4796 4797 4798 4799 4800 4801 4802 4803 4804 4805 4806 4807 4808 4809 4972 5122 5123 5124 5125 5126 5127 5128 5129 5130 5131 5132 5133 5134 5135 5136 5137 5138 5139 5140 5141 5142 5170 5177 Mo

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0996-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.