FDAClass IIJuly 27, 2016

OT1000 Series Orthopedic Surgical Tables recall

OT1000 Series Orthopedic Surgical Tables

Why was OT1000 Series Orthopedic Surgical Tables recalled?

STERIS has identified that the pivot pin assembly located on the table top may become loose preventing the table from articulating properly.

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?

OT1000, OT1100, and OT1200 Orthopedic Surgical Table

Product
OT1000 Series Orthopedic Surgical Tables
Recalling firm
Steris Corporation
Quantity
148
Distribution
AL;AK, AZ; AR; CA; CO; CT; DC; FL; GA; IL; IN; IA; NY; NJ; NC; OH; OK; OR; PA; PR; SC; TX; UT and VA. Foreign accounts: Canada; France; Korea; Panama; Qatar and Thailand.
Recall date
July 27, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls