Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.
Reported: March 11, 2015 Initiated: February 5, 2015 #Z-1232-2015
Product Description
Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.
Reason for Recall
Use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.
Details
- Recalling Firm
- Remel Inc
- Units Affected
- 24 packs (10 x 100 ml vials)
- Distribution
- US Distribution to the states of : MI, ND, SC, TN, and TX.
- Location
- Lenexa, KS
Frequently Asked Questions
What product was recalled? ▼
Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.. Recalled by Remel Inc. Units affected: 24 packs (10 x 100 ml vials).
Why was this product recalled? ▼
Use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 11, 2015. Severity: Moderate. Recall number: Z-1232-2015.
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