FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Cantrell Drug Calcium Chloride Recall

Calcium Chloride (20 mg/mL) in 0

Cantrell Drug Company · Little Rock, AR

Risk level
Class II
Reported by FDA
Dec 21, 2016
Recall ID
D-0186-2017
Check your lot numberHow we source this data

Summary

Cantrell Drug recalled Calcium Chloride starting Nov 18, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0186-2017 on Dec 21, 2016. Reason: Lack of Assurance of Sterility - the firm is recalling select sterile drug products. Status: Terminated.

Why it was recalled

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Product description

Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09

Lot numbers, UPCs & expiration codes

Lot: 168032

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-0186-2017
Classification
Class II
Status
Terminated
Recall initiated
Nov 18, 2016
FDA report date
Dec 21, 2016
Quantity
73 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Cantrell Drug Company

Original FDA data

Every field from FDA enforcement report D-0186-2017, exactly as published.

Show all FDA fields
City
Little Rock
State
AR
Status
Terminated
Country
United States
Event ID
75745
Address
7321 Cantrell Rd
Code information
Lot: 168032
Postal code
72207-4144
Report date
Dec 21, 2016
Product type
Drugs
Recall number
D-0186-2017
Classification
Class II
Recalling firm
Cantrell Drug Company
Product quantity
73 bags
Termination date
Apr 29, 2020
Reason for recall
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09
Distribution pattern
Nationwide
Recall initiation date
Nov 18, 2016
Initial firm notification
Press Release
Center classification date
Dec 13, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0186-2017, published Dec 21, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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.

How we source and update recall data · Report incorrect information

Other recent drug recalls