Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported June 11, 2025
BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers
During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching th…
Civco Medical Instruments Co. Inc. recalled BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) pr… — a moderate-severity action.
BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) pr… was recalled by Civco Medical Instruments Co. Inc. in June 11, 2025. Reason: During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle gui…. Check the official notice for the remedy. Verify recall #Z-1892-2025 with the FDA Devices before acting.
The recall
Civco Medical Instruments Co. Inc. issued this moderate-severity FDA Devices recall — During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle gui….
- Moderate
- severity level
- Class II
- classification
- June 11, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1892-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1892-2025) was formally reported on June 11, 2025, with the manufacturer initiating the action on May 1, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Civco Medical Instruments Co. Inc. is listed as the recalling firm, operating out of Kalona, IA. Federal records list the affected scope as 506 boxes.
The documented reason for this recall is: During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place. Distribution data in the federal record shows the product reached: OUS Distribution to countries of: Japan, Taiwan, France, Georgia, Germany and 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, 6 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 — 40,409 medical devices recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 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
506 boxes
Related Recalls
6
6 from same agency
Product description
BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers
Reason for recall
During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1892-2025 |
| Date reported | June 11, 2025 |
| Date initiated | May 1, 2025 |
| Recalling firm | Civco Medical Instruments Co. Inc. |
| Firm location | Kalona, IA |
| Affected scope | 506 boxes |
| Distribution | OUS Distribution to countries of: Japan, Taiwan, France, Georgia, Germany and Denmark |
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-1892-2025) 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? ▼
BX2 Needle Guide, Part Number 644-094, tool for performing needle-guided (or catheter) procedures with the use of diagnostic ultrasound transducers. Recalled by Civco Medical Instruments Co. Inc.. Units affected: 506 boxes.
Why was this product recalled? ▼
During the attachment of the needle guide to the covered probe, the tight tolerance and fit of the needle guide can cause a pinhole breach in the transducer cover when latching the guide in place.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 11, 2025. Severity: Moderate. Recall number: Z-1892-2025.
Where was the recalled product distributed? ▼
Distribution: OUS Distribution to countries of: Japan, Taiwan, France, Georgia, Germany and Denmark.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1892-2025) 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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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Devices, reported June 11, 2025.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.