BD MaxGuard Extension Set with 2 Needleless Y-Site recall
BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059
Why was BD MaxGuard Extension Set with 2 Needleless Y-Site recalled?
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may be compromised, and may result in potential leaks and risk of infection to the patient and healthcare worker.
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?
UDI-DI: 10885403237584, Lots: 22029431, 22029432
- Product
- BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059
- Recalling firm
- CAREFUSION
- Quantity
- 17,250
- Distribution
- US: TN, FL, LA, VA, MI, OH, NC, WA, UT, TX, NV, AL, AR, IA, MA, CO, NY, SC, IN, KY, MO, MD, PA, CA, IL, SD, GA, MS, AZ, WV, ID, WY, VT, NM, OR, NJ, OK, KS, MN
- Recall date
- September 28, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)