Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems; Multipac Anasthesia Breathing Systems - Product Usage: intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece.
FDA Recall Z-0753-2021 · Posted None
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Recalling FirmIntersurgical Inc
Recall StatusTerminated
Product CodeOFP
Date Initiated2020-11-11
Date Terminated2022-08-09
Product Quantity200 devices
Reason for Recall
The device was assembled with the incorrect exhalation port which can cause gas leakage.
Firm Action
Recall Strategy and Instruction:
1. Immediately discontinue use and quarantine any stock with the product/lot number described above in this recall notification.
2. If you have distributed any of these products, please immediately contact your customers, advise them of the recall situation and have them return their outstanding recalled stock to you.
3. Complete the Customer Product Recall Acknowledgement Form
a. Return the completed form via email to Intersurgical Inc. at
[email protected].
b. The subject line should contain Intersurgical Recall: Company name
c. Please note: If you do not have the recalled product in stock, please check
the appropriate box on the Customer Product Recall Acknowledgement
Form.
4. Once we receive your Customer Product Recall Acknowledgement Form,
Intersurgical Customer Support will issue a Return Goods Authorization
(RGA) Number for the amount of product you have on-hand to return.
a. Intersurgical will credit your account when the product is received.
Intersurgical is committed to providing high quality, safe and effective products. We sincerely apologize for any inconvenience this action may cause your operations. If you have any other questions, feel free to contact Customer Support at 800-828-9633 or email at [email protected].
Distribution:
Distribution began 09/02/2020
Distributed: 200 pieces
Root Cause
Process control
Distribution Pattern
All of the devices were shipped to the same distributor (McKesson).
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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