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Class III: unlikely to cause harmTerminated

Aaron Industries Well at Walgreens Wal-Tussin CF Max Recall

Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi-Symptom C…

Aaron Industries Inc · Lynwood, CA

Risk level
Class III
Reported by FDA
Mar 13, 2013
Recall ID
D-185-2013
Check your lot numberHow we source this data

Summary

Aaron Industries recalled Well at Walgreens Wal-Tussin CF Max starting Jan 18, 2013. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-185-2013 on Mar 13, 2013. Reason: Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution. Status: Terminated.

Why it was recalled

Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.

Product description

Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (237 mL) bottles, Distributed by: Walgreen Co, Deerfield, IL 60015 ---- NDC 0363-0229-08

Lot numbers, UPCs & expiration codes

Lot# 80798; FP-49-081-14870,

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-185-2013
Classification
Class III
Status
Terminated
Recall initiated
Jan 18, 2013
FDA report date
Mar 13, 2013
Quantity
6,108 bottles (509 cases)
Recall type
Voluntary: Firm initiated
Recalling firm
Aaron Industries Inc

Original FDA data

Every field from FDA enforcement report D-185-2013, exactly as published.

Show all FDA fields
City
Lynwood
State
CA
Status
Terminated
Country
United States
Event ID
64298
Address
11865 Alameda St
Address (line 2)
11840 S Alameda ST
Code information
Lot# 80798; FP-49-081-14870,
Postal code
90262-4022
Report date
Mar 13, 2013
Product type
Drugs
Recall number
D-185-2013
Classification
Class III
Recalling firm
Aaron Industries Inc
Product quantity
6,108 bottles (509 cases)
Termination date
Nov 1, 2013
Reason for recall
Presence of Precipitate; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles. If the product is shaken or warmed the white particles goes into the solution.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (237 mL) bottles, Distributed by: Walgreen Co, Deerfield, IL 60015 ---- NDC 0363-0229-08
Distribution pattern
Nationwide
Recall initiation date
Jan 18, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Mar 7, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-185-2013, published Mar 13, 2013. View the source record (openFDA) · FDA enforcement reports

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

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