Pilling Modular Verres Body/Obturator recall
Pilling Modular Verres Body/Obturator, Product Code 140880
Why was Pilling Modular Verres Body/Obturator recalled?
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).
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot K3
- Product
- Pilling Modular Verres Body/Obturator, Product Code 140880
- Recalling firm
- Teleflex Medical
- Quantity
- 8
- Distribution
- US Distribution to the state of : UT
- Recall date
- March 23, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)