Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported September 11, 2013
WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog number: W086 WASP is a fully automated system used to process microbiological specimens in liquid phase for the investigation of infectious microbes.
The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. Th…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Copan Italia recalled WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog… - a low-severity action.
WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog… was recalled by Copan Italia in September 11, 2013. Reason: The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upg…. Check the official notice for the remedy. Verify recall #Z-2131-2013 with the FDA Devices before acting.
The recall
Copan Italia issued this low-severity FDA Devices recall-The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upg….
- Low
- severity level
- 63 units
- affected scope
- Class III
- classification
- September 11, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2131-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2131-2013) was formally reported on September 11, 2013, with the manufacturer initiating the action on August 9, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Copan Italia is listed as the recalling firm, operating out of Brescia, N/A. Federal records list the affected scope as 63 units.
The documented reason for this recall is: The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary … Distribution data in the federal record shows the product reached: Worldwide Distribution - USA including Oregon and California., and the countries of France, Belgium, Italy, Denmark, Norway, Switzerland, Romania, Finland, Germany, South Africa, Canada, Ireland, UK, Sweden and Japan. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
63 units
Related Recalls
6
3 from same agency
Product description
WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog number: W086 WASP is a fully automated system used to process microbiological specimens in liquid phase for the investigation of infectious microbes.
Reason for recall
The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary from the manufacturer in order to eliminate the very low risk of rotation of the broth table when the door is open.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-2131-2013 |
| Date reported | September 11, 2013 |
| Date initiated | August 9, 2013 |
| Recalling firm | Copan Italia |
| Firm location | Brescia, N/A |
| Affected scope | 63 units |
| Distribution | Worldwide Distribution - USA including Oregon and California., and the countries of France, Belgium, Italy, Denmark, Norway, Switzerland, Romania, Finland, Germany, South Africa, Canada, Ireland, UK, Sweden and Japan |
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-2131-2013) 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? ▼
WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog number: W086 WASP is a fully automated system used to process microbiological specimens in liquid phase for the investigation of infectious microbes.. Recalled by Copan Italia. Units affected: 63 units.
Why was this product recalled? ▼
The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary from the manufacturer in order to eliminate the very low risk of rotation of the broth table when the door is open.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 11, 2013. Severity: Low. Recall number: Z-2131-2013.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - USA including Oregon and California., and the countries of France, Belgium, Italy, Denmark, Norway, Switzerland, Romania, Finland, Germany, South Africa, Canada, Ireland, UK, Sweden and Japan.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2131-2013) 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 September 11, 2013. 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.