Recall events
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Event 93233
Event summary
Timeline bucket September 29, 2023
Product types Device
Classifications Class II
Statuses Ongoing
Recalling firm wording Physio-Control, Inc.
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
10 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 10
LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051
Z-0296-2024
Recall number Z-0296-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0296-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52187]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873988022/ Serial number: 38370274
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36772]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 10
LIFEPAK 15, REF: 99577-000055, Part Number V15-2-000061
Z-0297-2024
Recall number Z-0297-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 8 yrs.
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0297-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9730]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873979426/ Serial number: 38290540 38291328 38315311 38315314 38324196 38324199 38332345 38898631
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33652]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 10
LIFEPAK 15, REF: 99577-000061, Part Number V15-2-000067
Z-0298-2024
Recall number Z-0298-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0298-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[40169]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873979358/ Serial number: 38166543
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33433]
FDA event record
· Exact recall-number query on openFDA
device · product 4 of 10
LIFEPAK 15, REF: 99577-001255, Part Number V15-2-001602
Z-0299-2024
Recall number Z-0299-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 5 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0299-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46350]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873911648/ Serial number: 40644322 40644323 40644331 42221204 42934131
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33730]
FDA event record
· Exact recall-number query on openFDA
device · product 5 of 10
LIFEPAK 15, REF: 99577-001373, Part Number V15-7-000002
Z-0300-2024
Recall number Z-0300-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0300-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52186]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873884331/ Serial number: 49618486
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34258]
FDA event record
· Exact recall-number query on openFDA
device · product 6 of 10
LIFEPAK 15, REF: 99577-001955, Part Number V15-5-000584 and V15-7-000020
Z-0301-2024
Recall number Z-0301-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 4 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0301-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[9726]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873871713/ Serial number: 44174756, 46013280, 46966395, 48149013
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[33473]
FDA event record
· Exact recall-number query on openFDA
device · product 7 of 10
LIFEPAK 15, REF: 99577-001956, Part Number V15-7-000021
Z-0302-2024
Recall number Z-0302-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 1 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0302-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5090]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873871706/ Serial number: 46687975
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36965]
FDA event record
· Exact recall-number query on openFDA
device · product 8 of 10
LIFEPAK 15, REF: 99577-001957, Part Number V15-5-000586 and V15-7-000022
Z-0303-2024
Recall number Z-0303-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 8 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0303-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52184]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873871690/ Serial number: 43393466 44142362 44739628 44742060 47821623 49025144 49663485 49887344
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36937]
FDA event record
· Exact recall-number query on openFDA
device · product 9 of 10
LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023
Z-0304-2024
Recall number Z-0304-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 1 unit
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0304-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[57509]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873871683/ Serial number: 48839976
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[34584]
FDA event record
· Exact recall-number query on openFDA
Recall number Z-0305-2024
Initiated September 29, 2023
Classification Class II
Status Ongoing
Quantity 2 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Unknown
An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0305-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[46352]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
Reason for recall Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Code information UDI: 00883873871669/ Serial number: 48433670 and 48744028
Distribution pattern US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[36947]
FDA event record
· Exact recall-number query on openFDA
