Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported November 15, 2017
Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.
The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mis…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Northgate Technologies, Inc. recalled Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9… - a moderate-severity action.
Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9… was recalled by Northgate Technologies, Inc. in November 15, 2017. Reason: The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to No…. Check the official notice for the remedy. Verify recall #Z-0073-2018 with the FDA Devices before acting.
The recall
Northgate Technologies, Inc. issued this moderate-severity FDA Devices recall-The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to No….
- Moderate
- severity level
- 186 units
- affected scope
- Class II
- classification
- November 15, 2017
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0073-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0073-2018) was formally reported on November 15, 2017, with the manufacturer initiating the action on May 24, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Northgate Technologies, Inc. is listed as the recalling firm, operating out of Elgin, IL. Federal records list the affected scope as 186.
The documented reason for this recall is: The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled product to be used with the inco… Distribution data in the federal record shows the product reached: US Distribution to the following states : MA, NE and TN and Internationally to 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 - 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 - 40,422 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
186
Related Recalls
6
0 from same agency
Product description
Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.
Reason for recall
The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled product to be used with the incorrect generator. Could Delay Care.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0073-2018 |
| Date reported | November 15, 2017 |
| Date initiated | May 24, 2017 |
| Recalling firm | Northgate Technologies, Inc. |
| Firm location | Elgin, IL |
| Affected scope | 186 |
| Distribution | US Distribution to the following states : MA, NE and TN and Internationally to 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-0073-2018) 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? ▼
Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.. Recalled by Northgate Technologies, Inc.. Units affected: 186.
Why was this product recalled? ▼
The inner and outer labels on the product contain incorrect reference number of 9-202-3751DS. According to Northgate Technologies, the resistor in the probe will not allow the mislabeled product to be used with the incorrect generator. Could Delay Care.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 15, 2017. Severity: Moderate. Recall number: Z-0073-2018.
Where was the recalled product distributed? ▼
Distribution: US Distribution to the following states : MA, NE and TN and Internationally to Canada..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0073-2018) 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 November 15, 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.