Apellis Pharmaceuticals, Inc. 2023-10-11 Health serious FDA
Health · FDA · Recall #FDA-Z-2653-2023
Apellis Injection Kit 29g Injection Needle -single use intended to inject fluids into, or… Recall
Issued October 11, 2023 · Apellis Pharmaceuticals, Inc.
In October 2023, Apellis Pharmaceuticals, Inc. recalled the Apellis Injection Kit 29g Injection Needle -single use intended to inject fluids into, or…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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
What you should do
- 1 Stop using Apellis Injection Kit 29g Injection Needle -single use intended to inject fluids into, or… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Apellis Pharmaceuticals, Inc. 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
- Apellis Pharmaceuticals, Inc.
- Category
- Health
- Recall date
- October 11, 2023
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-2653-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Apellis Pharmaceuticals, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.