Baxter Equipo de transferencia para DP MiniCap de vida recall
Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S
Why was Baxter Equipo de transferencia para DP MiniCap de vida recalled?
Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.
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?
All lot numbers within expiry
- Product
- Baxter Equipo de transferencia para DP MiniCap de vida util prolongada con pinza de torsion, 5C4482S
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 116,628 units
- Distribution
- Worldwide
- Recall date
- February 16, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)