Cantrell Drug fentaNYL citrate Recall: FDA Class I

Why it was recalled

Subpotent Drug

Product description

fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR

Lot numbers, UPCs & expiration codes

a) Lots: 148292, exp 11/9/15 and 150610, exp 1/6/16 and b) Lots: 6208, exp 9/16/15 and 6851, exp 1/19/16

Where it was sold

Nationwide

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-1156-2016
Classification: Class I
Status: Terminated
Recall initiated: Aug 21, 2015
FDA report date: Jul 13, 2016
Quantity: a) 564 syringes and b) 1146 syringes
Recall type: Voluntary: Firm initiated
Recalling firm: Cantrell Drug Company

Original FDA data

Every field from FDA enforcement report D-1156-2016, exactly as published.

Show all FDA fields

City: Little Rock
State: AR
Status: Terminated
Country: United States
Event ID: 72028
Address: 7321 Cantrell Rd
Code information: a) Lots: 148292, exp 11/9/15 and 150610, exp 1/6/16 and b) Lots: 6208, exp 9/16/15 and 6851, exp 1/19/16
Postal code: 72207-4144
Report date: Jul 13, 2016
Product type: Drugs
Recall number: D-1156-2016
Classification: Class I
Recalling firm: Cantrell Drug Company
Product quantity: a) 564 syringes and b) 1146 syringes
Termination date: Feb 3, 2017
Reason for recall: Subpotent Drug
Voluntary / mandated: Voluntary: Firm initiated
Product description: fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR
Distribution pattern: Nationwide
Recall initiation date: Aug 21, 2015
Initial firm notification: E-Mail
Center classification date: Jul 6, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1156-2016, published Jul 13, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

Cantrell Drug fentaNYL citrate in 0 Recall

Summary