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Terminated

Pilling Modular Verres Body/Obturator, Product Code 140880

FDA Recall Z-1178-2016 · Posted 2016-03-16

Recalling FirmTeleflex Medical
Recall StatusTerminated
Product CodeGDM
Date Initiated2015-01-08
Date Terminated2017-04-14
Product Quantity8

Reason for Recall

Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).

Firm Action

Teleflex sent an Medical Device Advisory Notification letter dated January 8, 2016, to all affected customers notifying them of the packaging error. Our records indicate that you have received products that are subject to this notification. Teleflex Medical 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 your local sales representative or Customer Service at [email protected] or 1-866-246-6990.

Root Cause

Packaging process control

Distribution Pattern

US Distribution to the state of : UT

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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