CAREFUSION 2022-09-28 Health serious FDA
Health · FDA · Recall #FDA-Z-1756-2022
BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold… Recall
Issued September 28, 2022 · CAREFUSION
In September 2022, CAREFUSION recalled the BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact CAREFUSION to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- CAREFUSION
- Category
- Health
- Recall date
- September 28, 2022
- Units affected
- Not reported
- Sold at
- 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,
- Recall number
- FDA-Z-1756-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- CAREFUSION has 2 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.