Why it was recalled
Lack of Assurance of Sterility
Product description
BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix, AZ 85085. NDC 42852-001-24
Lot numbers, UPCs & expiration codes
Lot # 138-20182408@58 BUD 12/22/2018
Where it was sold
Product was distributed throughout the United States.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0224-2019
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 31, 2018
- FDA report date
- Nov 14, 2018
- Quantity
- 911 syringes
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Avella of Deer Valley, Inc. Store 38
Original FDA data
Every field from FDA enforcement report D-0224-2019, exactly as published.
Show all FDA fields
- City
- Phoenix
- State
- AZ
- Status
- Terminated
- Country
- United States
- Event ID
- 81466
- Address
- 24416 N 19th Ave
- Code information
- Lot # 138-20182408@58 BUD 12/22/2018
- Postal code
- 85085-1887
- Report date
- Nov 14, 2018
- Product type
- Drugs
- Recall number
- D-0224-2019
- Classification
- Class II
- Recalling firm
- Avella of Deer Valley, Inc. Store 38
- Product quantity
- 911 syringes
- Termination date
- Jan 18, 2019
- Reason for recall
- Lack of Assurance of Sterility
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- BEVACIZUMAB 2.5 MG/0.1ML, pre-filled syringe (deliverable dose of 1.25MG in normject syringe) Repackaged by Avella Specialty Pharmacy, 24416 N 19th Avenue, Pheonix, AZ 85085. NDC 42852-001-24
- Distribution pattern
- Product was distributed throughout the United States.
- Recall initiation date
- Oct 31, 2018
- Initial firm notification
- Letter
- Center classification date
- Nov 7, 2018