Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported December 13, 2017
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix" system, which performs identification and susceptibility testing
Potential unexpected movement of robot arm
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Becton Dickinson & Co. recalled BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use… - a low-severity action.
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use… was recalled by Becton Dickinson & Co. in December 13, 2017. Reason: Potential unexpected movement of robot arm. Check the official notice for the remedy. Verify recall #Z-0198-2018 with the FDA Devices before acting.
The recall
Becton Dickinson & Co. issued this low-severity FDA Devices recall-Potential unexpected movement of robot arm.
- Low
- severity level
- 7 units
- affected scope
- Class III
- classification
- December 13, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0198-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0198-2018) was formally reported on December 13, 2017, with the manufacturer initiating the action on June 1, 2017. It is classified under Low severity (Class III), with a current status of Terminated. Becton Dickinson & Co. is listed as the recalling firm, operating out of Sparks, MD. Federal records list the affected scope as 7 units.
The documented reason for this recall is: Potential unexpected movement of robot arm Distribution data in the federal record shows the product reached: Worldwide Distribution - US including CA, NC & TN Internationally: Canada. 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
7 units
Related Recalls
6
3 from same agency
Product description
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix" system, which performs identification and susceptibility testing
Reason for recall
Potential unexpected movement of robot arm
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-0198-2018 |
| Date reported | December 13, 2017 |
| Date initiated | June 1, 2017 |
| Recalling firm | Becton Dickinson & Co. |
| Firm location | Sparks, MD |
| Affected scope | 7 units |
| Distribution | Worldwide Distribution - US including CA, NC & TN Internationally: Canada |
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-0198-2018) 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? ▼
BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples for use on the BD Phoenix" system, which performs identification and susceptibility testing. Recalled by Becton Dickinson & Co.. Units affected: 7 units.
Why was this product recalled? ▼
Potential unexpected movement of robot arm
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 13, 2017. Severity: Low. Recall number: Z-0198-2018.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - US including CA, NC & TN Internationally: Canada.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0198-2018) 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 13, 2017. 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.