FDAClass IIAugust 29, 2018

BuckyDiagnost Ceiling System recall

BuckyDiagnost Ceiling System (Stitching Patient Support) 704031

Why was BuckyDiagnost Ceiling System recalled?

The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial Number: 477195/SN11000090

Product
BuckyDiagnost Ceiling System (Stitching Patient Support) 704031
Recalling firm
Philips Medical Systems Gmbh, DMC
Distribution
US Nationwide; International to 66 countries
Recall date
August 29, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
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