FDAClass IIJuly 1, 2015

Steriseal-Cannula Ophthalmic recall

Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.

Why was Steriseal-Cannula Ophthalmic recalled?

The metal cannula attached to the handpiece can rotate and become dislodged from the plastic handpiece.

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?

Product #s: 157400; 257400; 157500; 257500

Product
Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece.
Recalling firm
Hill-Rom, Inc.
Quantity
66691 units
Distribution
Worldwide Distribution-US (nationwide) including the states of MI & PA, and the countries of Belgium, England, Italy, Czech Republic, Turkey, Greece, Ireland, Scotland, Spain, and Lebanon.
Recall date
July 1, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls