Stimulan Kit 10cc recall: Labeling Error
Stimulan Kit 10cc, Model 600-010 - Product Usage: intended for use as a bone void filler for voids or gaps that are not intrinsic to the stability of…
Why was Stimulan Kit 10cc recalled?
The product is mislabeled.
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 SK190610, Expiry June 2022
- Product
- Stimulan Kit 10cc, Model 600-010 - Product Usage: intended for use as a bone void filler for voids or gaps that are not intrinsic to the stability of…
- Recalling firm
- Biocomposites, Ltd.
- Quantity
- 54 boxes
- Distribution
- Worldwide distribution - US Nationwide in the Puerto Rico and the country of Costa Rica.
- Recall date
- December 30, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)