Baxter DISCPAC Syringe Tip Caps recall: Sterility Concern
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF H938693025, b) 100 pack REF H938673100
Why was Baxter DISCPAC Syringe Tip Caps recalled?
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
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?
a) 25 pack REF H938693025, UDI 00085412479965, ALL LOTS; b) 100 pack REF H938673100, UDI 00085412479798, ALL LOTS
- Product
- Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF H938693025, b) 100 pack REF H938673100
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 24,320 units
- Distribution
- Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
- Recall date
- August 31, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)