Zilretta recall
Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial, 5mL vials, Single-dose Kits, Rx Only, Manufactured for…
Why was Zilretta recalled?
Temperature Abuse: Product was stored at room temperature longer than 6 weeks and was inadvertently distributed instead of discarded
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: ZA19014, exp. date 05/2021 Only the specific lot distributed by Besse Medical are affected.
- Product
- Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial, 5mL vials, Single-dose Kits, Rx Only, Manufactured for…
- Recalling firm
- Flexion Therapeutics, Inc.
- Quantity
- 792 kits
- Distribution
- Nationwide within the United States only lots distributed by Besse Medical are affected.
- Recall date
- July 8, 2020
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)