Apellis Injection Kit 29g Injection Needle -single use intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin and either an 18-gauge or a 19-gauge 5 micron filter needle. Ref: IVT-KIT-29G
FDA Recall Z-2653-2023 · Posted 2023-09-29
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Recalling FirmApellis Pharmaceuticals, Inc.
Recall StatusOpen, Classified
Product CodeFMI
Date Initiated2023-08-22
Product Quantity61,943 units
Reason for Recall
19-gauge x 1" inch filter needles showed appearances of a small fraction of non-preferred characteristics. A causal relationship has not been established between the structural variations in this 19-gauge filter needle and the rare events of retinal vasculitis
Firm Action
Apellis issued Medical Device Field Correction letters via email on 8/22/23 to Healthcare Practitioners and Distributors/Specialty Distributors and Pharmacy/ Logistics. The communication to the Healthcare Practitioners also includes update on the rare events of retinal vasculitis with real world use of SYFOVRE (pegcetacoplan injection). A causal relationship has not been established between the 19-gauge needle and the rare events of retinal vasculitis in the real world.
Letter states reason for recall, health risk and action to take:
Actions to be taken by the Customer/Distributor:
Please note that as part of this field action, you are requested to:
" Confirm your availability and participation by sending back an email to acknowledge receipt of this message.
" Immediately cease distribution of the below injection kit lots and place any remaining inventory of the lots On Hold.
" Provide a summary of current on-hand inventory of the injection kit lots below.
" Provide a distribution report of the injection kit lots including customer name/address, lot shipped, quantity shipped, and date.
Please provide the Distribution report in a maximum time of four business hours.
Apellis will also be recommending that practitioners discontinue use of, and dispose, any remaining injection kits that contain the specific 19-gauge filter needle and recommend they instead use the injection kits containing the 18-gauge filter needle already in distribution.
Apellis is now exclusively distributing injection kits with the 18-gauge filter needle.
If you need to place a supplemental order to replace quarantined lots, please place them immediately through your normal ordering process and Apellis will expedite shipping replacement injection kits./
Apellis will also be notifying physicians that if they do not have an injection kit with the 18-gauge filter needle, they may request a new kit at no cost by emailing [email protected] or contacting their Apellis Territory Business Mana
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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