FDAClass IIDecember 4, 2019

Pro-stim 10cc Injectable recall: Sterility Concern

PRO-STIM 10cc INJECTABLE, Part Number 86SR0410

Why was Pro-stim 10cc Injectable recalled?

The firm discovered a lack of adequate documentation confirming sterility on certain products.

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 Number 1564697

Product
PRO-STIM 10cc INJECTABLE, Part Number 86SR0410
Recalling firm
Wright Medical Technology, Inc.
Quantity
19 units
Distribution
US and Norway, Italy, Germany, France, South Africa, UK, Taiwan, Austria, Japan, Turkey, Denmark, Canada, Switzerland, Belgium, The Netherlands, Spain
Recall date
December 4, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls