Severity
Moderate
FDA Devices recall · Reported November 16, 2016
The floor locking cylinders are contained in the base of the Schaerer 7300 model surgical tables. The cylinders were manufactured with the incorrect "O" ring which may cause the c…
Schaerer Medical USA Inc recalled Replacement floor locking cylinders for the Schaerer model 7300 surgical tables. Replacem… - a moderate-severity action.
Replacement floor locking cylinders for the Schaerer model 7300 surgical tables. Replacem… was recalled by Schaerer Medical USA Inc in November 16, 2016. Reason: The floor locking cylinders are contained in the base of the Schaerer 7300 model surgical tables. The cylinde…. Check the official notice for the remedy. Verify recall #Z-0372-2017 with the FDA Devices before acting.
The recall
Schaerer Medical USA Inc issued this moderate-severity FDA Devices recall-The floor locking cylinders are contained in the base of the Schaerer 7300 model surgical tables. The cylinde….
Sourced from official FDA Devices enforcement records. Verify recall #Z-0372-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-0372-2017) was formally reported on November 16, 2016, with the manufacturer initiating the action on September 27, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Schaerer Medical USA Inc is listed as the recalling firm, operating out of Cincinnati, OH. Federal records list the affected scope as 10 replacement cylinders..
The documented reason for this recall is: The floor locking cylinders are contained in the base of the Schaerer 7300 model surgical tables. The cylinders were manufactured with the incorrect "O" ring which may cause the cylinder to leak. Distribution data in the federal record shows the product reached: Worldwide Distribution - US Nationwide in the states of: CA, CT, FL, IA, IN, MI, MN, MO, OH, PA, and VA Replcement cylinders wre distributed. 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.
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.
Severity
Moderate
Affected scope
10 replacement cylinders.
Related Recalls
6
3 from same agency
Replacement floor locking cylinders for the Schaerer model 7300 surgical tables. Replacement cylinders are part number 85118. Product Usage: The cylinders are used to lock the surgical table in place.
The floor locking cylinders are contained in the base of the Schaerer 7300 model surgical tables. The cylinders were manufactured with the incorrect "O" ring which may cause the cylinder to leak.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0372-2017 |
| Date reported | November 16, 2016 |
| Date initiated | September 27, 2016 |
| Recalling firm | Schaerer Medical USA Inc |
| Firm location | Cincinnati, OH |
| Affected scope | 10 replacement cylinders. |
| Distribution | Worldwide Distribution - US Nationwide in the states of: CA, CT, FL, IA, IN, MI, MN, MO, OH, PA, and VA Replcement cylinders wre distributed |
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.
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.
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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 16, 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.