Introcan Safety IV Catheter 22G x 1'' PUR with Wings. The affected catalogs and lot numbers: Catalog Number 4253540 - Lo
FDA device recall Z-1092-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Braun,B Medical Inc
- Reason for recall
- 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 taken
- The recalling firm received a product complaint of a mixed 18G Catheters with 22G Catheters.
- Root cause
- Other
- Status
- Terminated
- Product code
- FOZ
- Quantity affected
- 86 units
- 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
- Date initiated
- 2004-03-19
- Date posted
- 2004-07-20
- Date terminated
- 2004-09-21
- Location
- Allentown, PA
Monitor recalls programmatically
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| INTROCAN SAFETY IV CATHETER (K020785) | B.Braun Medical, Inc. | 2002-08-28 |
| INTROCAN SAFETY IV CATHETER (K982805) | B.Braun Medical, Inc. | 1999-01-14 |