Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported December 3, 2014
Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.
Some versions of Application Specifications (App Spec) are incompatible with m2000sp system software version 6.0 and 7.0. This issue will cause Error Code 9000 (An unexpected erro…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Abbott Molecular recalled Abbott m2000sp, an automated system for performing sample preparation for nucleic acid te… - a moderate-severity action.
Abbott m2000sp, an automated system for performing sample preparation for nucleic acid te… was recalled by Abbott Molecular in December 3, 2014. Reason: Some versions of Application Specifications (App Spec) are incompatible with m2000sp system software version …. Check the official notice for the remedy. Verify recall #Z-0463-2015 with the FDA Devices before acting.
The recall
Abbott Molecular issued this moderate-severity FDA Devices recall-Some versions of Application Specifications (App Spec) are incompatible with m2000sp system software version ….
- Moderate
- severity level
- Class II
- classification
- December 3, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0463-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0463-2015) was formally reported on December 3, 2014, with the manufacturer initiating the action on October 23, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Abbott Molecular is listed as the recalling firm, operating out of Des Plaines, IL. Federal records list the affected scope as 9 CD ROMs (US); 1,273 CD ROMs (Foreign).
The documented reason for this recall is: Some versions of Application Specifications (App Spec) are incompatible with m2000sp system software version 6.0 and 7.0. This issue will cause Error Code 9000 (An unexpected error has occurred: Software error) to be ge… Distribution data in the federal record shows the product reached: Worldwide distribution. US nationwide (CA, CT, FL, NC, PA, SC, and DC), Algeria , Australia , Austria , Belgium , Bosnia and Herzegovina , Cameroon , Canada , Chad , Colombia , Costa Rica , Croatia , Denmark …. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
9 CD ROMs (US); 1,273 CD ROMs (Foreign)
Related Recalls
6
3 from same agency
Product description
Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.
Reason for recall
Some versions of Application Specifications (App Spec) are incompatible with m2000sp system software version 6.0 and 7.0. This issue will cause Error Code 9000 (An unexpected error has occurred: Software error) to be generated when the Available Reagent Packs screen is selected.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0463-2015 |
| Date reported | December 3, 2014 |
| Date initiated | October 23, 2014 |
| Recalling firm | Abbott Molecular |
| Firm location | Des Plaines, IL |
| Affected scope | 9 CD ROMs (US); 1,273 CD ROMs (Foreign) |
| Distribution | Worldwide distribution. US nationwide (CA, CT, FL, NC, PA, SC, and DC), Algeria , Australia , Austria , Belgium , Bosnia and Herzegovina , Cameroon , Canada , Chad , Colombia , Costa Rica , Croatia , Denmark , Egypt , Ethiopia… |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0463-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Abbott m2000sp, an automated system for performing sample preparation for nucleic acid testing.. Recalled by Abbott Molecular. Units affected: 9 CD ROMs (US); 1,273 CD ROMs (Foreign).
Why was this product recalled? ▼
Some versions of Application Specifications (App Spec) are incompatible with m2000sp system software version 6.0 and 7.0. This issue will cause Error Code 9000 (An unexpected error has occurred: Software error) to be generated when the Available Reagent Packs screen is selected.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 3, 2014. Severity: Moderate. Recall number: Z-0463-2015.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution. US nationwide (CA, CT, FL, NC, PA, SC, and DC), Algeria , Australia , Austria , Belgium , Bosnia and Herzegovina , Cameroon , Canada , Chad , Colombia , Costa Rica , Croatia , Denmark , Egypt , Ethiopia , Finland , France , Germany , Greece , Guinea , Honduras , Hong Kong , India , Indonesia , Ireland , Israel , Italy , Japan , Kenya , Korea , Lithuania , Mali , Mexico , Netherlands , New Zealand , Nigeria , Norway , Pakistan , Paraguay , Poland , Portugal , Romania , Russia , Saudi Arabia , Senegal , Slovenia , South Africa , Spain , Sweden , Switzerland , Taiwan , Tanzania , Thailand , Turkey , Uganda , Ukraine , United Arab Emirates, United Kingdom , Vietnam.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0463-2015) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported December 3, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.