FDAClass IIMarch 23, 2022

DREAMTOME 49-30MM/260CM Material Number: M00584010 recall: Sterility Concern

DREAMTOME 49-30MM/260CM Material Number: M00584010

Why was DREAMTOME 49-30MM/260CM Material Number: M00584010 recalled?

Sterility of device is compromised due to a sterile barrier breach

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA 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?

Lot Numbers: 27566790 27641143 27852432 GTIN: 8714729778233

Product
DREAMTOME 49-30MM/260CM Material Number: M00584010
Recalling firm
Boston Scientific Corporation
Quantity
472 units
Distribution
Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Canada, Botswana, China, Czech Republic, Denmark, Finland, France, Germany, Great Britain, Greece, Ireland, Italy, Japan, Korea, Kuwait, Latvia, Lebanon, Mauritius, Morocco, Namibia, Netherlands, New Zealand, Norway, Poland, Portugal, Qatar, Romania, Russian Fed., Saudi Arabia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Unit. Arab Emir.
Recall date
March 23, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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