Medical Device Recall: Z-0010-06

FDA Recalls dataset · Firm: Abbott Laboratories, Inc · Status: Terminated

Recall Action Class: N/A Date Initiated: 2005-09-14 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0010-06.

Recall Res Number
Z-0010-06
Recalling Firm / Manufacturer
FEI Number
1628664
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2005-09-14
Date Posted
2005-10-06
Date Terminated
2007-09-25
Product Code
JJE
Event Number
33460
Product Quantity
1,107 units
Product Description ARCHITECT c8000 Analyzer System Processing Module, a fully automated, random access, clinical chemistry analyzer which utilizes spectrophotometry (monochromatic and bichromatic modes of measurement) for photometric based determinations.

Reason for Recall Software deficiency causing potential shift in absorbance readings for test results.

Action Details Firm sent device correction letter to consignees on 9/14/2005.

Distribution Pattern Nationwide and 21 foreign countries. Foreign countries: Mexico, Guatemala, Venezuela, Colombia, Ecuador, Chile, Uruguay, Argentina, Brazil, Puerto Rico, Jamaica, San Salvador, Canada, Germany, Singapore, China, Thailand, Australia, New Zealand, Panama, and Grand Cayman

Code Information / Serial Numbers All serial numbers, List number 1G06-01

Related Establishments / Registrations

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