D-1675-2012 Class II Terminated
FDA drug recall D-1675-2012 was initiated by Dukal Corp. on June 14, 2012 and is designated Class II. Reason for recall: Microbial contamination of Non Sterile Product; contamination with Burkholderia cepacia (manufacturer) The recall status is terminated (terminated June 21, 2013).
Recall Details
- Product Type
- Drugs
- Report Date
- September 26, 2012
- Initiation Date
- June 14, 2012
- Termination Date
- June 21, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
ZEE Antiseptic Wipes, First Aid Antiseptic, Benzalkonium chloride 0.133% (effective concentration), over the counter; supplied in 10 (item 2633), 50 (items 0204 and 02040 [sold in Canada only]) and 100 (item 0271) wipes per box distributed by ZEE MEDICAL, INC., Irvine, CA
Reason for Recall
Microbial contamination of Non Sterile Product; contamination with Burkholderia cepacia (manufacturer)
Distribution Pattern
Nationwide
Code Information
Antiseptic wipes shipped since July 02, 2009. Lots: JT14509, JT15209, JT20609, JT20909, JT23709, JT27809, JT32809, JT00710, JT15810, JT18310, JT18810, JT23210, JT25810, JT27610, JT31510, JT35610, JT35911, JT04811, JT05311, JT11811, JT15211, JT15911, JT18211, JT18211, JT21511-1, JT26311, JT30711, JT22011-1, JT01012, JT04112, JT06512, JT07512, JT07710, JT14509, JT15209, JT21409, JT20609, JT33009, JT00710, JT18810, JT23210, JT35911, JT05311, JT11811, JT26311, JT01012, JT14509, JT15209, JT20609, JT15209, JT23709, JT27809, JT00710, JT00710, JT18310, JT18810, JT23210, JT23210, JT27610, JT31510, JT05809, JT14509, JT15209, JT21209, JT27809, JT12510, JT15810, JT18310, JT11811, JT13211, JT15911, JT35911, JT01012, JT30711