fentaNYL citrate 1000 mcg (10 mcg/mL) 100 mL Cassette in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025011001

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Lot #: 041317S1, Exp 10/10/2017; 041817S1, Exp 10/15/2017; 042017S1, 10/17/2017; 042517S1, 10/22/2017; 042717S1, Exp 10/24/2017; 050217S1, Exp 10/29/2017; 050417S2, Exp 10/31/2017; 050917S1, 11/5/2017; 051117S1, 051117S4,11/7/2017; 051617S1, 11/12/2017; 051817S1, Exp 11/14/2017; 052317S1, Exp 11/19/2017; 053017S1, Exp 11/26/2017; 060617S1, Exp 12/3/2017; 060917S1, Exp 12/6/2017; 061317S1, Exp 12/10/2017; 061517S2, Exp 12/12/2017; 062017S1, Exp 12/17/2017; 062217S1, Exp 12/19/2017; 062717S1, Exp 12/24/2017; 62817S1, Exp 12/25/2017; 070417S1, Exp 12/31/2017; 070517S1, Exp 1/1/2018; 071317S1, Exp 1/7/2018; 071817S2, Exp 1/14/2018; 072017S1,Exp 1/16/2018; 72517S2, Exp 1/21/2018; 080817S1, Exp 2/4/2018; 080917S1, Exp 2/5/2018; 081617S1, Exp 2/12/2018; 081717S1, Exp 2/13/2018.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Banner Pharmacy Services, LLC
Reason for Recall:
Lack of Assurance of Sterility.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

fentaNYL citrate 1000 mcg (10 mcg/mL) 100 mL Cassette in 0.9% Sodium Chloride, Rx Only, Banner Health Compounding Pharmacy 7300 W Detroit St Chandler, AZ 85226, NDC 7025011001

Product Codes/Lot Numbers:

Lot #: 041317S1, Exp 10/10/2017; 041817S1, Exp 10/15/2017; 042017S1, 10/17/2017; 042517S1, 10/22/2017; 042717S1, Exp 10/24/2017; 050217S1, Exp 10/29/2017; 050417S2, Exp 10/31/2017; 050917S1, 11/5/2017; 051117S1, 051117S4,11/7/2017; 051617S1, 11/12/2017; 051817S1, Exp 11/14/2017; 052317S1, Exp 11/19/2017; 053017S1, Exp 11/26/2017; 060617S1, Exp 12/3/2017; 060917S1, Exp 12/6/2017; 061317S1, Exp 12/10/2017; 061517S2, Exp 12/12/2017; 062017S1, Exp 12/17/2017; 062217S1, Exp 12/19/2017; 062717S1, Exp 12/24/2017; 62817S1, Exp 12/25/2017; 070417S1, Exp 12/31/2017; 070517S1, Exp 1/1/2018; 071317S1, Exp 1/7/2018; 071817S2, Exp 1/14/2018; 072017S1,Exp 1/16/2018; 72517S2, Exp 1/21/2018; 080817S1, Exp 2/4/2018; 080917S1, Exp 2/5/2018; 081617S1, Exp 2/12/2018; 081717S1, Exp 2/13/2018.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0017-2018

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