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Class 3 Device Recall Reliamed |
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Date Initiated by Firm |
August 16, 2010 |
Date Posted |
September 17, 2010 |
Recall Status1 |
Terminated 3 on January 24, 2011 |
Recall Number |
Z-2426-2010 |
Recall Event ID |
56564 |
Product Classification |
Bag, Stomal - Product Code GDS
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Product |
Reliamed Odor Eliminator Drops (8 oz, 4 oz, 1 oz package sizes) |
Code Information |
Reliamed Odor Eliminator Drops, 8 oz Part #ZR8OZED, UPC Code 84216701352 Lots: H09010, M09008, M09011, M09016, N09011, M09020, N09015, N09022, N09023, A10001, E10051, B10018, D10008, E09022. Reliamed Odor Eliminator Drops, 4 oz Part #ZR4OZED, UPC Code 84216701652 Lots: H09010, M09006, M09016. Reliamed Odor Eliminator Drops, 1 oz Part # ZR1OZED, UPC Code 84216701342 Lots: N09022. |
Recalling Firm/ Manufacturer |
BioMed Laboratories 2414 Executive Dr # 102 Garland TX 75041-6123
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For Additional Information Contact |
Greg White 972-989-7646
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Manufacturer Reason for Recall |
The product may contain the mold Aspergillus ssp.
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FDA Determined Cause 2 |
Material/Component Contamination |
Action |
Biomed Laboratories, Inc. of Garland, TX is conducting a recall of the Reliamed Odor Eliminator Drops, Securi-T Ostomy Deodorant, and the Safe n' Simple (Sn'S) Ostomy Appliance Deodorant. Lots being recalled were distributed between June 9, 2009 though June 28, 2010. Biomed will work with their 3 consignees to inform sub-distributors and down to any firm that keeps the product in stock to have the product removed from further distribution and returned. If there are any questions or concerns, please contact Biomed Laboratories, Inc. at (972) 282-8008 or email them at biomedlabs.net. |
Quantity in Commerce |
33,772 Units (27,148 8oz bottles. 3,492 4oz bottles. 3,132 1oz bottles). |
Distribution |
OH, FL, MI |
Total Product Life Cycle |
TPLC Device Report
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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