Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,
FDA Recall Z-0075-2023 · Posted 2022-10-14
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Recalling FirmTELEFLEX LLC
Recall StatusOpen, Classified
Product CodeCAH
Date Initiated2022-08-29
Product Quantity355 units
Reason for Recall
Incidents of device splitting or detaching during use
Firm Action
Teleflex, Inc. sent an URGENT MEDICAL DEVICE RECALL notice by Fedex 2-day mail on 08/29/2022. the notice described the problem, listed the complaints and requested the following actions be taken:
Medical facilities:
1. Immediately check your inventory for product within the scope of this
recall. Cease use and distribution of affected product and immediately
quarantine the affected product.
2. If you have impacted product, mark the applicable checkbox on the Acknowledgement Form and contact Teleflex Customer Service by calling the phone number provided.
Teleflex Customer Service will issue a return goods authorization (RGA) number to
you. Write the RGA number in the Acknowledgement Form and
return form by email to [email protected].
3. If you do not have impacted product, mark the applicable checkbox on the Acknowledgement Form and return the form to Teleflex at [email protected].
4. Teleflex (or your local dealer) will issue a credit note upon receipt of the returned affected product.
Distributors:
1. Provide this recall notice to all customers who have received impacted product. Each of your customers must complete the Acknowledgement Form and return it to you.
2. Immediately check your inventory for impacted product. Cease use and distribution of impacted product and immediately quarantine the affected product. You may return all product in scope.
3. As a distributor, you must confirm to Teleflex that you have completed the
field activity outlined in actions 1 and 2 of this Action List Number 2. Upon completion of your actions, please forward the completed Acknowledgement Form to Teleflex Customer Service.
Important - Please ensure you only list batch numbers in scope of this recall notice when
completing this form.
4. If you have further distributed product outside of your country, please notify Teleflex
Customer Service by email to [email protected]
On October 28, 2022, the firm sent an updated recall notice with the expansion to additional
Root Cause
Under Investigation by firm
Distribution Pattern
US nationwide distribution
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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