Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported February 17, 2016
Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Richard Wolf Medical Instruments Corp. recalled Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachme… - a moderate-severity action.
Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachme… was recalled by Richard Wolf Medical Instruments Corp. in February 17, 2016. Reason: Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proxim…. Check the official notice for the remedy. Verify recall #Z-0789-2016 with the FDA Devices before acting.
The recall
Richard Wolf Medical Instruments Corp. issued this moderate-severity FDA Devices recall-Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proxim….
- Moderate
- severity level
- Class II
- classification
- February 17, 2016
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0789-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0789-2016) was formally reported on February 17, 2016, with the manufacturer initiating the action on November 25, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Richard Wolf Medical Instruments Corp. is listed as the recalling firm, operating out of Vernon Hills, IL. Federal records list the affected scope as Ten units.
The documented reason for this recall is: Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional. Distribution data in the federal record shows the product reached: Distributed in Washington.. 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
Ten units
Related Recalls
6
3 from same agency
Product description
Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.
Reason for recall
Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0789-2016 |
| Date reported | February 17, 2016 |
| Date initiated | November 25, 2015 |
| Recalling firm | Richard Wolf Medical Instruments Corp. |
| Firm location | Vernon Hills, IL |
| Affected scope | Ten units |
| Distribution | Distributed in Washington. |
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-0789-2016) 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? ▼
Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment or accessory to the air-powered device intended for use during surgical procedures to cut hard tissue or bone and soft tissue. General hospital and plastic surgery use.. Recalled by Richard Wolf Medical Instruments Corp.. Units affected: Ten units.
Why was this product recalled? ▼
Weak weld in the reusable rotary blade/abrader (burr) may result in inner part breaks at the distal or proximal end making the product dysfunctional.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 17, 2016. Severity: Moderate. Recall number: Z-0789-2016.
Where was the recalled product distributed? ▼
Distribution: Distributed in Washington..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0789-2016) 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 February 17, 2016. 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.