Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported May 22, 2013
Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.
On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodi…
Covidien LLC recalled Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit. - a low-severity action.
Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit. was recalled by Covidien LLC in May 22, 2013. Reason: On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is re…. Check the official notice for the remedy. Verify recall #Z-1304-2013 with the FDA Devices before acting.
The recall
Covidien LLC issued this low-severity FDA Devices recall-On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is re….
- Low
- severity level
- Class III
- classification
- May 22, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1304-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1304-2013) was formally reported on May 22, 2013, with the manufacturer initiating the action on April 12, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Covidien LLC is listed as the recalling firm, operating out of Mansfield, MA. Federal records list the affected scope as 52363 distributed.
The documented reason for this recall is: On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in … Distribution data in the federal record shows the product reached: Worldwide distribution: USA (nationwide) and in the country of: Panama.. 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
52363 distributed
Related Recalls
6
3 from same agency
Product description
Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.
Reason for recall
On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-1304-2013 |
| Date reported | May 22, 2013 |
| Date initiated | April 12, 2013 |
| Recalling firm | Covidien LLC |
| Firm location | Mansfield, MA |
| Affected scope | 52363 distributed |
| Distribution | Worldwide distribution: USA (nationwide) and in the country of: Panama. |
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-1304-2013) 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? ▼
Curity Staple Remover Kit; Product Code: 66701. Staple Remover Kit.. Recalled by Covidien LLC. Units affected: 52363 distributed.
Why was this product recalled? ▼
On March 26, 2013 Covidien received a recall notice from one of their suppliers CareFusion. CareFusion is recalling a variety of OTC drug products including the 10% Povidone Iodine SEPP Applicator which is utilized in specific convenience kits.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 22, 2013. Severity: Low. Recall number: Z-1304-2013.
Where was the recalled product distributed? ▼
Distribution: Worldwide distribution: USA (nationwide) and in the country of: Panama..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1304-2013) 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 May 22, 2013. 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.