FDAClass IIJanuary 4, 2023

Pilling Wecksorb Cylindrical Sponges recall: Sterility Concern

Pilling Wecksorb Cylindrical Sponges

Why was Pilling Wecksorb Cylindrical Sponges recalled?

Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.

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?

Catalog Number: 200400, Lot Number: 22B0395

Product
Pilling Wecksorb Cylindrical Sponges
Recalling firm
TELEFLEX LLC
Quantity
1,000 units
Distribution
Domestic distribution to IL, MS, PA, TN.
Recall date
January 4, 2023
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls