RecallRadar

FDA Device recall Z-0761-2016

VS200 radiographic Cassette Holder or Wall Stand

On 2016-02-17 the FDA classified a Class II recall of VS200 radiographic Cassette Holder or Wall Stand by Del Medical, citing the wall stand cassette holder can suddenly fall to the bottom of its travel, near the ground and contact patient.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0761-2016
ClassificationClass II
Statusterminated
Initiated2015-12-03
Published2016-02-17
Last updated2026-09-13 11:54 UTC
CompanyDel Medical
DistributionUS

Product

VS200 radiographic Cassette Holder or Wall Stand. For use in radiology department.

Reason

The wall stand cassette holder can suddenly fall to the bottom of its travel, near the ground and contact patient.

Identifiers

code_info
Product # Serial # 110-5010G1 , 00504-0214 110-5010G1 , 00855-0414 110-5010G1 , 00182-0114 110-5010G1 , 00108-0114…Product # Serial # 110-5010G1 , 00504-0214 110-5010G1 , 00855-0414 110-5010G1 , 00182-0114 110-5010G1 , 00108-0114 110-5010G1 , 00479-0214 110-5010G1 , 00014-0114 110-5010G1 , 00251-0214 110-5010G1 , 00854-0414 110-5010G1 , 00505-0214 110-5010G1 , 00342-0214 110-5010G1 , 00477-0214 110-5010G1 , 00184-0114 110-5010G1 , 00248-0214 110-5010G1 , 00588-0314 110-5010G1 , 00852-0414 110-5010G1 , 00107-0114 110-5010G1 , 00183-0114 110-5010G1 , 00480-0214 110-5010G1 , 00503-0214 110-5010G1 , 00443-0214 110-5010G1 , 00853-0414 110-5010G1 , 00941-0414 110-5010G1 , 00013-0114 110-5010G1 , 00343-0214 110-5010G1 , 00478-0214 110-5010G1 , 00249-0214 110-5010G1 , 00185-0114 110-5010G1 , 00442-0214 110-5010G1 , 00632-0314 110-5010G1 , 00475-0214 110-5010G1 , 00507-0214 110-5010G1 , 00015-0114 110-5010G1 , 00631-0314 110-5010G1 , 01008-0514 110-5010G1 , 00635-0314 110-5010G1 , 00011-0114 110-5010G1 , 00012-0114 110-5010G1 , 00345-0214 110-5010G1 , 00590-0314 110-

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-0761-2016%22

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