Baxter DISCPAC Syringe Tip Caps recall: Sterility Concern
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
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 H93869025, UDI 00085412479965, ALL LOTS; b) 100 pack, REF H938674100, UDI 00085412479811, ALL LOTS; c) 100 pack, REF H93869100, UDI 00085412478944, ALL LOTS
- Product
- Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Green: a) 25 pack, REF H93869025, b) 100 pack, REF H938674100, c) 100 pack, REF H93869100
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 168390 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)