Medical Device Recall: Z-0042-2012

FDA Recalls dataset · Firm: Exalenz Bioscience Ltd Hamaayan 4 Modiin Israel · Status: Terminated

Recall Action Class: N/A Date Initiated: 2011-06-07 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0042-2012.

Recall Res Number
Z-0042-2012
Recalling Firm / Manufacturer
FEI Number
3005772418
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2011-06-07
Date Posted
2011-10-12
Date Terminated
2012-07-06
Product Code
MSQ
Event Number
59891
Product Quantity
1240 units
Product Description IDkit:HP" Breath Test for Detection of H. pylori, Manufactured by: Exalenz Bioscience Ltd 4 Ha' maayan St. Modiin, Israel 71700, Distributed by: Exalenz Bioscience Inc., 1313 N. Market St., Sute 5100, Wilmington, DE 19808 USA Product Usage: The IDkit:HP Two Test System is intended for use in the qualitative detection of urease associated with Helicobacter pylori in the human stomach and as an aid in initial diagnosis and post treatment monitoring of H. pylori infection in adult patients. Urea Breath Tests are well established as reliable, non-invasive methods for detecting H. pylori. They are highly endorsed by various medical societies as the test of choice for initial detection as well as for post-treatment testing.

Reason for Recall The product is in violation of the FD&C Act in that it was illegally marketed without proper clearance (no 510(k) submitted).

Action Details The firm, Exalenz Bioscience Ltd. notified consignees located in the United States of the recall by telephone, electronic mail, or written correspondence between June 9, 2011 and June 30, 2011. The letter informed consignees that Exalenz will immediately cease marketing the IDkit:HP TWO test in the United States. Consignees were instructed to return shipment of the IDkit:HP TWO test kits that they have in their possession to the companys US warehouse. For question call the VP of North American Sales at 704-770-6162 or VP of Marketing at 617-794-6936.

Distribution Pattern Nationwide Distribution (USA) - including the states of: FL, IL, LA, MA, MS, NY, TN, TX and VA.

Code Information / Serial Numbers Reorder No. AC00028, Lot numbers: 11-071, 11-0561, 10-00018 and 10-00017.

Related Establishments / Registrations

Public Record Disclaimer

This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

Account Required Full available specs will require a free AvaSpecs account.