Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 24, 2012
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.
This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Moog Medical Devices Group recalled ***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Inf… - a moderate-severity action.
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Inf… was recalled by Moog Medical Devices Group in October 24, 2012. Reason: This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which…. Check the official notice for the remedy. Verify recall #Z-0072-2013 with the FDA Devices before acting.
The recall
Moog Medical Devices Group issued this moderate-severity FDA Devices recall-This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which….
- Moderate
- severity level
- Class II
- classification
- October 24, 2012
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0072-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0072-2013) was formally reported on October 24, 2012, with the manufacturer initiating the action on September 26, 2012. It is classified under Moderate severity (Class II), with a current status of Terminated. Moog Medical Devices Group is listed as the recalling firm, operating out of Salt Lake City, UT. Federal records list the affected scope as 12,000 sets.
The documented reason for this recall is: This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administ… Distribution data in the federal record shows the product reached: Nationwide Distribution including California. 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
12,000 sets
Related Recalls
6
3 from same agency
Product description
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.
Reason for recall
This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0072-2013 |
| Date reported | October 24, 2012 |
| Date initiated | September 26, 2012 |
| Recalling firm | Moog Medical Devices Group |
| Firm location | Salt Lake City, UT |
| Affected scope | 12,000 sets |
| Distribution | Nationwide Distribution including California |
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-0072-2013) 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? ▼
***This recall is being conducted due to an incomplete recall for RES 57829*** Curlin Infusion Administration Set, REF 340-4165, Sterile EO, The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications.. Recalled by Moog Medical Devices Group. Units affected: 12,000 sets.
Why was this product recalled? ▼
This recall is the same issue for the FDA processed recall initiated by Moog Medical Devices on 1/25/11 which was related to customers reporting unclearable Air-In-Line alarm with specific lot numbers of Curlin Administration Sets used with Curlin Ambulatory Infusion Pumps. The lots associated with this recall were inadvertently omitted from the original recall which has since been terminated by
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 24, 2012. Severity: Moderate. Recall number: Z-0072-2013.
Where was the recalled product distributed? ▼
Distribution: Nationwide Distribution including California.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0072-2013) 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 October 24, 2012. 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.