FDA Medical Device Recalls (openFDA)
Allergan Sales, LLC: Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only
- Recall number
- Z-1694-2024
- Recalling firm
- Allergan Sales, LLC
- Product
- Keller Funnel 2, REF: HA-001, STERILEEO, Rx Only,
- Status
- Open, Classified
- Initiated
- 2024-03-14
- Posted
- 2024-04-29
- Terminated
- not on file
- Reason
- Their is a potential that breast implants lack the lubricious coating that allows them to slide through the funnels during the implantation procedure.
- Root cause
- Process design
- Action
- Between the dates of March 28, 2024 - April 1, 2024, Allergan Aesthetics (Allergan Sales LLC) issued a "Urgent Medical Device Recall" notification to affected consignees via FedEx. Allergan asked consignees to take the following actions: 1. If you have the affected product, discontinue further use and quarantine products prior to return. 2. Conduct a physical count of the affected product in your possession and record the count on the enclosed Business Response Form. 3. Send the Business Response Form to Qualanex LLC, AbbVie s third-party recall processor, via email within five (5) business days of receipt. To ensure we are able to account for all recalled product, it is imperative that you return the form. Please return the Business Response Form even if you have no recalled product to return. 4. Upon receipt of your Business Response Form, Qualanex LLC will issue a Return Authorization Form. When returning the recalled products, include the Return Authorization form and attach the prepaid Authorized Return shipping label to the outside of the return carton. Return the recalled product to: Qualanex, LLC 1410 Harris Rd. Libertyville, IL 60048 5. Please do not return any products that are not the subject of this recall. On 7/15/2025, updated recall notices were emailed to customers informing them of an additional impacted lot.
- Quantity
- 10837
- Distribution
- US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.
- Lot, serial or model codes
- UDI: 10888628043725 / Lot #: 23B35C, 23B41C, 23B42C, 23C05C, 23C06C, 23D01C, 24C12C
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KDD
- Firm FEI
- 2011068
- Firm city
- Irvine
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28