BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171
Reported: September 28, 2022 Initiated: August 1, 2022 #Z-1759-2022
Product Description
BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171
Reason for Recall
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.
Details
- Recalling Firm
- CAREFUSION
- Units Affected
- 100
- 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
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171. Recalled by CAREFUSION. Units affected: 100.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 28, 2022. Severity: Moderate. Recall number: Z-1759-2022.
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