Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported September 25, 2019
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reverse…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
CooperSurgical, Inc. recalled LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures. - a low-severity action.
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures. was recalled by CooperSurgical, Inc. in September 25, 2019. Reason: Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect exp…. Check the official notice for the remedy. Verify recall #Z-2545-2019 with the FDA Devices before acting.
The recall
CooperSurgical, Inc. issued this low-severity FDA Devices recall-Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect exp….
- Low
- severity level
- 5K units
- affected scope
- Class III
- classification
- September 25, 2019
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2545-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2545-2019) was formally reported on September 25, 2019, with the manufacturer initiating the action on August 19, 2019. It is classified under Low severity (Class III), 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 4930 units.
The documented reason for this recall is: Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed. Distribution data in the federal record shows the product reached: USA: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, & WV. Distribution US nationwide, Canada, Colo…. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
4930 units
Related Recalls
6
3 from same agency
Product description
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
Reason for recall
Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-2545-2019 |
| Date reported | September 25, 2019 |
| Date initiated | August 19, 2019 |
| Recalling firm | CooperSurgical, Inc. |
| Firm location | Trumbull, CT |
| Affected scope | 4930 units |
| Distribution | USA: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, & WV. Distribution US nationwide, Canada, Colombia, Japan, & Malay… |
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-2545-2019) 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? ▼
LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.. Recalled by CooperSurgical, Inc.. Units affected: 4930 units.
Why was this product recalled? ▼
Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 25, 2019. Severity: Low. Recall number: Z-2545-2019.
Where was the recalled product distributed? ▼
Distribution: USA: AK, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, & WV. Distribution US nationwide, Canada, Colombia, Japan, & Malaysia.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2545-2019) 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 September 25, 2019. 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.