Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Labetalol 20mg Recalled by Avella of Deer Valley, Inc. Store 38 Due to Labeling: Incorrect or Missing Lot and/or Exp Date:The...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Avella of Deer Valley, Inc. Store 38 directly.
Affected Products
Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-822-71.
Quantity: 2,840 4mL syringes
Why Was This Recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date:The product labels contain a Two-Dimensional ( 2D ) barcode that, when scanned, reveals information specific to the batch of the labeled product, including Expiration Date. The expiration date included within these 2D barcodes is incorrect and does not match the correct expiration date listed on the face of the label itself.
Where Was This Sold?
Distribution to 13 states: Alabama, Arizona, California, Colorado, Florida, Idaho, Michigan, Minnesota, North Carolina, New Jersey, Oregon, Pennsylvania, Texas.
About Avella of Deer Valley, Inc. Store 38
Avella of Deer Valley, Inc. Store 38 has 50 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report