Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported June 24, 2015
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80
A diaphragm size 80 labeled box was incorrectly packaged with a size 85.
CooperSurgical, Inc. recalled MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80 - a moderate-severity action.
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80 was recalled by CooperSurgical, Inc. in June 24, 2015. Reason: A diaphragm size 80 labeled box was incorrectly packaged with a size 85.. Check the official notice for the remedy. Verify recall #Z-1814-2015 with the FDA Devices before acting.
The recall
CooperSurgical, Inc. issued this moderate-severity FDA Devices recall-A diaphragm size 80 labeled box was incorrectly packaged with a size 85..
- Moderate
- severity level
- 200 units
- affected scope
- Class II
- classification
- June 24, 2015
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1814-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1814-2015) was formally reported on June 24, 2015, with the manufacturer initiating the action on May 20, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. CooperSurgical, Inc. is listed as the recalling firm, operating out of Trumbull, CT. Federal records list the affected scope as 200 units.
The documented reason for this recall is: A diaphragm size 80 labeled box was incorrectly packaged with a size 85. Distribution data in the federal record shows the product reached: AK, CA, DC, FL, IL, ME, MT, NE, NJ, NM, NY, OK, OR, P A, VA, W A, and WI Foreign: CANADA, ENGLAND, and POLAND. 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
200 units
Related Recalls
6
3 from same agency
Product description
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80
Reason for recall
A diaphragm size 80 labeled box was incorrectly packaged with a size 85.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1814-2015 |
| Date reported | June 24, 2015 |
| Date initiated | May 20, 2015 |
| Recalling firm | CooperSurgical, Inc. |
| Firm location | Trumbull, CT |
| Affected scope | 200 units |
| Distribution | AK, CA, DC, FL, IL, ME, MT, NE, NJ, NM, NY, OK, OR, P A, VA, W A, and WI Foreign: CANADA, ENGLAND, and POLAND |
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-1814-2015) 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? ▼
MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80. Recalled by CooperSurgical, Inc.. Units affected: 200 units.
Why was this product recalled? ▼
A diaphragm size 80 labeled box was incorrectly packaged with a size 85.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 24, 2015. Severity: Moderate. Recall number: Z-1814-2015.
Where was the recalled product distributed? ▼
Distribution: AK, CA, DC, FL, IL, ME, MT, NE, NJ, NM, NY, OK, OR, P A, VA, W A, and WI Foreign: CANADA, ENGLAND, and POLAND.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1814-2015) 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 June 24, 2015. 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.