Severity
Critical
CriticalClass IOngoing
FDA Devices recall · Reported May 24, 2023
Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010
Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery ru…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Icu Medical Inc recalled Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Numbe… - a critical-severity action.
Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Numbe… was recalled by Icu Medical Inc in May 24, 2023. Reason: Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity…. Check the official notice for the remedy. Verify recall #Z-1565-2023 with the FDA Devices before acting.
The recall
Icu Medical Inc issued this critical-severity FDA Devices recall-Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity….
- Critical
- severity level
- 29K units
- affected scope
- Class I
- classification
- May 24, 2023
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1565-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1565-2023) was formally reported on May 24, 2023, with the manufacturer initiating the action on March 22, 2023. It is classified under Critical severity (Class I), with a current status of Ongoing. Icu Medical Inc is listed as the recalling firm, operating out of Lake Forest, IL. Federal records list the affected scope as 28656 units.
The documented reason for this recall is: Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease earlier in the batter… Distribution data in the federal record shows the product reached: worldwide. 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
28656 units
Related Recalls
6
3 from same agency
Product description
Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010
Reason for recall
Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease earlier in the battery lifecycle than expected.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | Z-1565-2023 |
| Date reported | May 24, 2023 |
| Date initiated | March 22, 2023 |
| Recalling firm | Icu Medical Inc |
| Firm location | Lake Forest, IL |
| Affected scope | 28656 units |
| Distribution | worldwide |
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-1565-2023) 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.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. 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? ▼
Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010. Recalled by Icu Medical Inc. Units affected: 28656 units.
Why was this product recalled? ▼
Due to a manufacturing defect from the battery supplier, affected batteries may experience a loss of capacity earlier in the battery lifecycle than expected and overall battery runtime may decrease earlier in the battery lifecycle than expected.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 24, 2023. Severity: Critical. Recall number: Z-1565-2023.
Where was the recalled product distributed? ▼
Distribution: worldwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1565-2023) 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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 24, 2023. 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.