Why it was recalled
Microbial Contamination of a Non-Sterile Products: The product had a positive Staphylococcus aureus test result.
Product description
Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone Laboratories, Memphis, TN 38101-2026, UPC 0 70596 00422 5.
Lot numbers, UPCs & expiration codes
Lot #: 9AD5
Where it was sold
Nationwide and Canada
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-0726-2016
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Feb 8, 2016
- FDA report date
- Mar 2, 2016
- Quantity
- 134 cases of 12 bottles/case
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Keystone Laboratories Inc
Original FDA data
Every field from FDA enforcement report D-0726-2016, exactly as published.
Show all FDA fields
- City
- Memphis
- State
- TN
- Status
- Terminated
- Country
- United States
- Event ID
- 73284
- Address
- 1103 Kansas St
- Code information
- Lot #: 9AD5
- Postal code
- 38106-1913
- Report date
- Mar 2, 2016
- Product type
- Drugs
- Recall number
- D-0726-2016
- Classification
- Class II
- Recalling firm
- Keystone Laboratories Inc
- Product quantity
- 134 cases of 12 bottles/case
- Termination date
- May 25, 2016
- Reason for recall
- Microbial Contamination of a Non-Sterile Products: The product had a positive Staphylococcus aureus test result.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone Laboratories, Memphis, TN 38101-2026, UPC 0 70596 00422 5.
- Distribution pattern
- Nationwide and Canada
- Recall initiation date
- Feb 8, 2016
- Initial firm notification
- Letter
- Center classification date
- Feb 22, 2016