Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, one
FDA device recall Z-1474-2014 · posted 2014-04-18 · Terminated
Recall details
- Recalling firm
- Remel Inc
- Reason for recall
- A reagent contained within the product may return false negative results.
- Action taken
- The recalling firm initiated a recall by issuing letters dated 3/17/14 via regular mail to their customers.
- Root cause
- Under Investigation by firm
- Status
- Terminated
- Product code
- LIB
- Quantity affected
- 2/50-test boxes
- Distribution
- Distribution was made to CA, FL, IL, MA, ME, NJ, PA, TN, TX, VA, and VT. There was no foreign/military/government distribution.
- Date initiated
- 2014-03-17
- Date posted
- 2014-04-18
- Date terminated
- 2014-12-11
- Location
- Lenexa, KS
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