Teleflex Medical Recalls Pilling Modular Verres Body/Obturator Due to Packaging Error
Teleflex Medical is recalling 8 units of Pilling Modular Verres Body/Obturator (Product Code 140880) in Utah because customers were incorrectly provided with a different product code.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class II, but the source text identifies the issue as a packaging error involving the wrong product code being shipped. There are no reported injuries, illnesses, or hazards explicitly named in the source text, fitting the criteria for a low-severity documentation or packaging issue.
Plain-English summary
Teleflex Medical is recalling 8 units of the Pilling Modular Verres Body/Obturator, Product Code 140880. The recall was initiated due to a packaging error where 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).
The affected units were distributed in the state of Utah. The specific lot number for the recalled product is K3.
Consumers who have purchased or received this product should stop using it and contact Teleflex Medical for further instructions.
The recalled product
- Product
- Pilling Modular Verres Body/Obturator, Product Code 140880
- Manufacturer
- Teleflex Medical
- Hazard
- Affected units
- 8
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot K3
Distribution
Distributed in 1 state:
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