Forcep recall: Sterility Concern
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
Why was Forcep recalled?
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
DYNJ04048, UDI-DI: 10193489195248(each), 20193489195245(case), Lot Number: 2023112290
- Product
- FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
- Recalling firm
- Medline Industries, LP
- Quantity
- 53 units
- Distribution
- US Nationwide distribution in the states CA, CO, IL, KS, and MI.
- Recall date
- December 24, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)