Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TUMARK Q Recalled by Somatex Medical Technologies GmbH Due to There is a potential risk of puncture to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Somatex Medical Technologies GmbH directly.
Affected Products
TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE
Quantity: N/A
Why Was This Recalled?
There is a potential risk of puncture to the packaging material which can compromise the devices sterility, making it non-sterile.
Where Was This Sold?
This product was distributed to 1 state: NY
About Somatex Medical Technologies GmbH
Somatex Medical Technologies GmbH has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report