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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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High RiskFDA Drug
Medications & Supplements/Prescription Drugs

Avella of Deer Valley, Inc. Store 38: Sterile Injectable Drugs Recalled Due to Lack of Sterility Assurance

Agency Publication Date: November 2, 2018
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Summary

Avella of Deer Valley, Inc. Store 38 is recalling 2,340 units of various sterile injectable medications, including Morphine, Fentanyl, Hydromorphone, and Phenylephrine. These prescription drugs were distributed in bags and syringes nationwide and are being recalled because there is no guarantee that the products are sterile. Using a non-sterile injectable drug can lead to serious, life-threatening infections, particularly in hospitalized or vulnerable patients. These products were produced at the Phoenix, Arizona facility and were distributed to healthcare facilities across the United States.

Risk

The lack of sterility assurance means the medications may contain bacteria or other contaminants. When injected directly into the bloodstream or body, these contaminants can cause severe infections, sepsis, or other life-threatening medical complications.

What You Should Do

  1. Identify if you have any of the affected products by checking for these specific lot numbers and expiration dates: Morphine (1 mg/mL) 100 mL bags: Lot 7/10/18 0415 24110P (Exp 11/07/2018) and Lot 7/25/18 0247 24110P (Exp 11/22/2018); Fentanyl (10 mcg/mL) 1 mL syringes: Lot 8/8/18 0200 15-21070S (Exp 11/06/2018).
  2. Identify if you have the following bags: Hydromorphone (0.2 mg/mL) 100 mL bags: Lot 8/27/18 0215 22110P (Exp 12/10/2018); Phenylephrine 25 mg in 250 mL bags: Lot 138-20182308@88 (Exp 11/06/2018); and Phenylephrine 30 mg in 250 mL bags: Lot 138-20180409@55 (Exp 11/18/2018).
  3. Immediately stop using any medications that match the affected lot numbers and expiration dates.
  4. Contact your healthcare provider or pharmacist immediately for guidance if you have been administered any of these recalled products or if you have them in your possession.
  5. Return any unused recalled product to the pharmacy or facility where it was obtained for a refund.
  6. Contact Avella of Deer Valley, Inc. Store 38 at 24416 N 19th Ave, Phoenix, AZ for further instructions regarding the return of these medications.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy return

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Morphine (1 mg/mL) in NS 100 mL Bag
Model:
D-0131-2019
Lot Numbers:
7/10/18 0415 24110P (Exp 11/07/2018)
7/25/18 0247 24110P (Exp 11/22/2018)
Date Ranges: Expiration 11/07/2018, Expiration 11/22/2018
Product: Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe)
Model:
D-0132-2019
Lot Numbers:
8/8/18 0200 15-21070S (Exp 11/06/2018)
Date Ranges: Expiration 11/06/2018
Product: Hydromorphone (0.2 mg/mL) in NS 100 mL Bag
Model:
D-0133-2019
Lot Numbers:
8/27/18 0215 22110P (Exp 12/10/2018)
Date Ranges: Expiration 12/10/2018
Product: Phenylephrine 25 mg added to NS 250 mL Bag
Model:
D-0134-2019
Lot Numbers:
138-20182308@88 (Exp 11/06/2018)
Date Ranges: Expiration 11/06/2018
Product: Phenylephrine 30 mg added to NS 250 mL Bag
Model:
D-0135-2019
Lot Numbers:
138-20180409@55 (Exp 11/18/2018)
Date Ranges: Expiration 11/18/2018

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81413
Status: Resolved
Manufacturer: Avella of Deer Valley, Inc. Store 38
Sold By: Advanced Pharma, Inc.; Avella of Houston; Avella of Deer Valley, Inc. #38
Manufactured In: United States
Units Affected: 5 products (1,360 bags; 20 syringes; 360 bags; 300 bags; 300 bags)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.