Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported November 20, 2019
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
TriMed Inc. recalled TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is … - a moderate-severity action.
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is … was recalled by TriMed Inc. in November 20, 2019. Reason: The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.. Check the official notice for the remedy. Verify recall #Z-0358-2020 with the FDA Devices before acting.
The recall
TriMed Inc. issued this moderate-severity FDA Devices recall-The spring on the PEG-Extender can rust due to the type of steel used to manufacture it..
- Moderate
- severity level
- Class II
- classification
- November 20, 2019
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0358-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0358-2020) was formally reported on November 20, 2019, with the manufacturer initiating the action on September 28, 2018. It is classified under Moderate severity (Class II), with a current status of Ongoing. TriMed Inc. is listed as the recalling firm, operating out of Santa Clarita, CA. Federal records list the affected scope as 1,903 Peg Guide Extenders.
The documented reason for this recall is: The spring on the PEG-Extender can rust due to the type of steel used to manufacture it. Distribution data in the federal record shows the product reached: Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden.. 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
1,903 Peg Guide Extenders
Related Recalls
6
3 from same agency
Product description
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Reason for recall
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-0358-2020 |
| Date reported | November 20, 2019 |
| Date initiated | September 28, 2018 |
| Recalling firm | TriMed Inc. |
| Firm location | Santa Clarita, CA |
| Affected scope | 1,903 Peg Guide Extenders |
| Distribution | Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden. |
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-0358-2020) 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? ▼
TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.. Recalled by TriMed Inc.. Units affected: 1,903 Peg Guide Extenders.
Why was this product recalled? ▼
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 20, 2019. Severity: Moderate. Recall number: Z-0358-2020.
Where was the recalled product distributed? ▼
Distribution: Distribution was nationwide. There was military distribution but no government distribution. Foreign distribution was made to Australia, China, South Africa, and Sweden..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0358-2020) 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 November 20, 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.