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Terminated

Terumo Needle, 30G x 1/2", Product Code NN3013R

FDA Recall Z-2006-2019 · Posted None

Recalling FirmTerumo Medical Corporation
Recall StatusTerminated
Product CodeFMI
Date Initiated2019-02-08
Date Terminated2020-05-08
Product Quantity81,000

Reason for Recall

There is a potential for a loss of package integrity that may compromise the sterility of the product.

Firm Action

Urgent Voluntary Medical Device Recall notification letters dated 2/8/19 were sent to customers.

Root Cause

Packaging

Distribution Pattern

The products were distributed to the following US states: FL, IN, KS, KY, MA, MO, NH, NV, PA, SC, TN, and TX.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K121607TERUMO(R) NEEDLETerumo (Philippines) Corporation · 2012-11-08

Official Source

View FDA Recall →

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

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