Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported April 9, 2014
IMMULITE 2000; IMMULITE 2000XPi; VersaCell The IMMULITE 2000 systems are continuous random-access instruments that perform chemiluminescent immunoassays. These instruments use serum, plasma, or urine samples for in vitro diagnostic testing. The VersaCell system is a robotic sample-moving device that supports an interface to a number of laboratory analysis systems, such as the IMMULITE 2000
There is a potential for incorrect results to be reported from processing of a sample tube.
Siemens Medical Solutions Diagnostics recalled IMMULITE 2000; IMMULITE 2000XPi; VersaCell The IMMULITE 2000 systems are continuous ra… - a moderate-severity action.
IMMULITE 2000; IMMULITE 2000XPi; VersaCell The IMMULITE 2000 systems are continuous ra… was recalled by Siemens Medical Solutions Diagnostics in April 9, 2014. Reason: There is a potential for incorrect results to be reported from processing of a sample tube.. Check the official notice for the remedy. Verify recall #Z-1316-2014 with the FDA Devices before acting.
The recall
Siemens Medical Solutions Diagnostics issued this moderate-severity FDA Devices recall-There is a potential for incorrect results to be reported from processing of a sample tube..
- Moderate
- severity level
- 1K units
- affected scope
- Class II
- classification
- April 9, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1316-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1316-2014) was formally reported on April 9, 2014, with the manufacturer initiating the action on February 3, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Siemens Medical Solutions Diagnostics is listed as the recalling firm, operating out of Flanders, NJ. Federal records list the affected scope as 1006 units.
The documented reason for this recall is: There is a potential for incorrect results to be reported from processing of a sample tube. Distribution data in the federal record shows the product reached: Nationwide and Foreign Distribution.. 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
1006 units
Related Recalls
6
3 from same agency
Product description
IMMULITE 2000; IMMULITE 2000XPi; VersaCell The IMMULITE 2000 systems are continuous random-access instruments that perform chemiluminescent immunoassays. These instruments use serum, plasma, or urine samples for in vitro diagnostic testing. The VersaCell system is a robotic sample-moving device that supports an interface to a number of laboratory analysis systems, such as the IMMULITE 2000
Reason for recall
There is a potential for incorrect results to be reported from processing of a sample tube.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1316-2014 |
| Date reported | April 9, 2014 |
| Date initiated | February 3, 2014 |
| Recalling firm | Siemens Medical Solutions Diagnostics |
| Firm location | Flanders, NJ |
| Affected scope | 1006 units |
| Distribution | Nationwide and Foreign Distribution. |
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-1316-2014) 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? ▼
IMMULITE 2000; IMMULITE 2000XPi; VersaCell The IMMULITE 2000 systems are continuous random-access instruments that perform chemiluminescent immunoassays. These instruments use serum, plasma, or urine samples for in vitro diagnostic testing. The VersaCell system is a robotic sample-moving device that supports an interface to a number of laboratory analysis systems, such as the IMMULITE 2000. Recalled by Siemens Medical Solutions Diagnostics. Units affected: 1006 units.
Why was this product recalled? ▼
There is a potential for incorrect results to be reported from processing of a sample tube.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 9, 2014. Severity: Moderate. Recall number: Z-1316-2014.
Where was the recalled product distributed? ▼
Distribution: Nationwide and Foreign Distribution..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1316-2014) 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 April 9, 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.