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Class III: unlikely to cause harmTerminated

Akorn Halyard 24-Hour Oral Care Kit q4 Recall

Halyard 24-Hour Oral Care Kit q4, contains 2x15 mL Unit Dose Cups 0

Akorn Inc · Lake Forest, IL

Risk level
Class III
Reported by FDA
Aug 23, 2017
Recall ID
D-1090-2017
Check your lot numberHow we source this data

Summary

Akorn recalled Halyard 24-Hour Oral Care Kit q4 starting Jul 12, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1090-2017 on Aug 23, 2017. Reason: Crystallization with subpotent out of specification assay results for chlorhexidine. Status: Terminated.

Why it was recalled

Crystallization with subpotent out of specification assay results for chlorhexidine.

Product description

Halyard 24-Hour Oral Care Kit q4, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97014

Lot numbers, UPCs & expiration codes

Lots: 0202635072, 0202635073, EXP 06-2018; 0202630205, 0202630206, EXP 07-2018; 0202630203, 0202630204, 0202642217, 0202642218, 0202642219, 0202647410, 0202647411, EXP 08-2018; 0202647409, 0202647412, 0202653431, 0202653432, EXP 09-2018.

Where it was sold

Nationwide in the USA

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-1090-2017
Classification
Class III
Status
Terminated
Recall initiated
Jul 12, 2017
FDA report date
Aug 23, 2017
Quantity
101,952 15 mL unit dose cups
Recall type
Voluntary: Firm initiated
Recalling firm
Akorn Inc

Original FDA data

Every field from FDA enforcement report D-1090-2017, exactly as published.

Show all FDA fields
City
Lake Forest
State
IL
Status
Terminated
Country
United States
Event ID
77822
Address
1925 W Field Ct
Code information
Lots: 0202635072, 0202635073, EXP 06-2018; 0202630205, 0202630206, EXP 07-2018; 0202630203, 0202630204, 0202642217, 0202642218, 0202642219, 0202647410, 0202647411, EXP 08-2018; 0202647409, 0202647412, 0202653431, 0202653432, EXP 09-2018.
Postal code
60045-4862
Report date
Aug 23, 2017
Product type
Drugs
Recall number
D-1090-2017
Classification
Class III
Recalling firm
Akorn Inc
Product quantity
101,952 15 mL unit dose cups
Termination date
Jun 19, 2018
Reason for recall
Crystallization with subpotent out of specification assay results for chlorhexidine.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Halyard 24-Hour Oral Care Kit q4, contains 2x15 mL Unit Dose Cups 0.12% Chlorhexidine Gluconate Oral Rinse. Manufactured by Halyard Health Inc., 5405 Windward Parkway, Alpharetta, GA 30004. Distributed by Halyard Sales, LLC Alpharetta, GA 30004. REF # 97014
Distribution pattern
Nationwide in the USA
Recall initiation date
Jul 12, 2017
Initial firm notification
Letter
Center classification date
Aug 14, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1090-2017, published Aug 23, 2017. View the source record (openFDA) · FDA enforcement reports

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

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