RecallRadar

FDA Device recall Z-1264-2018

IMRIS ORT200, Removable Operating Room Table, Part Numbers: (a) 113821-000 (b) 113821-600 (c) 114148-000 (d) 114148-600

On 2018-04-04 the FDA classified a Class II recall of IMRIS ORT200, Removable Operating Room Table, Part Numbers: (a) 113821-000 (b) 113821-600 (c) 114148-000 (d) 114148-600 by Deerfield Imaging, citing the Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1264-2018
ClassificationClass II
Statusterminated
Initiated2018-02-23
Published2018-04-04
Last updated2026-09-13 11:54 UTC
CompanyDeerfield Imaging
Distributionn/a

Product

IMRIS ORT200, Removable Operating Room Table, Part Numbers: (a) 113821-000 (b) 113821-600 (c) 114148-000 (d) 114148-600

Reason

The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.

Identifiers

code_info
(a) 113821-000, Serial Numbers: 10006997, 10002220 (b) 113821-600, Serial Numbers: 10002692,10006152, 10007192, 1000…(a) 113821-000, Serial Numbers: 10006997, 10002220 (b) 113821-600, Serial Numbers: 10002692,10006152, 10007192, 10006991, 10003754, 10006997, 10004513 (c) 114148-000, Serial Numbers: 10004463, 10005189, 10005190, 10006891, 10004997, 10004327 (d) 114148-600, Serial Numbers: 10005201, 10006891

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-1264-2018%22

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