FDA Recall
Terminated
Introcan Safety IV Catheter 22G x 1'' PUR with Wings. The affected catalogs and lot numbers: Catalog Number 4253540 - Lot number 3G26258U02 Catalog Number 4253540 - Lot number 3G27258U02
Recall: Z-1092-04
·
Initiated March 19, 2004
Recall
- Recall Number
- Z-1092-04
- Event Number
- 28912
- Firm
- Braun, B Medical Inc
- FEI Number
- 2523676
- Product Code
- FOZ
- Status
- Terminated
- Root Cause
- Other
- Initiated
- March 19, 2004
- Posted
- July 20, 2004
- Terminated
- September 21, 2004
- Address
- 901 Marcon Blvd, Allentown, PA, 18109-9512
Description
Introcan Safety IV Catheter 22G x 1'' PUR with Wings. The affected catalogs and lot numbers: Catalog Number 4253540 - Lot number 3G26258U02 Catalog Number 4253540 - Lot number 3G27258U02
Reason
Mislabeled product. The recalling firm received a complaint that a box of Introcan Safety Catheters, (22G x 1 inch) contained mixed 18G catheters with the same lot number.
Action
The recalling firm received a product complaint of a mixed 18G Catheters with 22G Catheters.
Distribution
The affected recalling units were distributed nationwide to the following states: AZ, CA, GA, IL, IN, MD, OH, OK, OR, MA, MI, NC, NJ, NY, OR, PA, TX, UT, VA, WI
Quantity
86 units