Ear Loop Procedure Masks With Plastic Shield, For one time use only, Glass-Free, Reorder No. 2202, packed in a cardboard
FDA device recall Z-0573-03 · posted 2003-02-25 · Terminated
Recall details
- Recalling firm
- Dynarex Corporation
- Reason for recall
- Product labeled as 'latex free' but recent tests indicate that it contains minute amounts of latex.
- Root cause
- Other
- Status
- Terminated
- Product code
- FXX
- Quantity affected
- 396 cases (50 masks per box, 4 boxes per case)
- Distribution
- Medical/dental supply distributors nationwide and Puerto Rico, and 2 foreign accounts in the Bahamas.
- Date initiated
- 2002-12-31
- Date posted
- 2003-02-25
- Date terminated
- 2012-08-30
- Location
- Orangeburg, NY
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