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LIFELINE FIRST AID LLC

US

Last updated September 17, 2026

Information

Country
US
Address
6710 SW McEwan Rd, Lake Oswego, OR, 97035
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3002714597
DUNS Number
—

Catalogue (40)

DeviceModel / ReferenceRegistriesClassStatus
Lifeline LLICE-CAMP
FDA UDI
Class IActive
Gm 5143GM
FDA UDI
NActive
Aaa 4330AAA
FDA UDI
NActive
Big 5 4409-B5
FDA UDI
NActive
Aaa 4184AAA
FDA UDI
NActive
Realtree 4450
FDA UDI
NActive
Lifeline 4312
FDA UDI
Class IActive
Lifeline 4120
FDA UDI
NActive
Aaa 4180AAA
FDA UDI
NActive
Lifeline 4409
FDA UDI
NActive
Lifeline 4432
FDA UDI
NActive
Lifeline 4060
FDA UDI
NActive
Lifeline 4404
FDA UDI
NActive
Lifeline LLICE-SM
FDA UDI
Class IActive
Volkswagen 000093108L9B9
FDA UDI
NActive
Lifeline 4145
FDA UDI
NActive
Aaa 4284AAA
FDA UDI
NActive
Lifeline 4147
FDA UDI
NActive
Aaa 4366AAA
FDA UDI
NActive
Realtree 4452
FDA UDI
NActive
Gm 5143GM-ELEC
FDA UDI
NActive
Lifeline 4406
FDA UDI
NActive
Lifeline 4150
FDA UDI
NActive
Lifeline 4076
FDA UDI
NActive
Subaru 5896SUB
FDA UDI
NActive
Aaa 4390AAA
FDA UDI
NActive
Lifeline 4434
FDA UDI
Class IActive
Lifeline 4146
FDA UDI
NActive
Lifeline 4107
FDA UDI
NUnknown
Aaa 4365AAA
FDA UDI
NActive
Lifeline 4402
FDA UDI
NActive
Gm 5145GM
FDA UDI
NActive
Lifeline 4408
FDA UDI
NActive
Aaa 4388AAA
FDA UDI
NActive
Subaru 5895SUB
FDA UDI
NActive
Lifeline 4971
FDA UDI
NUnknown
Realtree 4451
FDA UDI
NActive
Aaa 4182AAA
FDA UDI
NActive
Gm 5191GM
FDA UDI
NActive
Realtree 4453
FDA UDI
NActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (7)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
May 16, 2016Z-2133-2016—terminated

Cadillac First Aid Kit is recalled because it contains the CPR Shield with One Way Valve and Barrier Filter (mask) and this mask is cleared only for prescription use and is not cleared for over-the-counter (OTC) use.

May 16, 2016Z-2132-2016—terminated

First aid kits or rescue kits are recalled because they contains the CPR Shield with One Way Valve and Barrier Filter (mask) and this mask is cleared only for prescription use and is not cleared for over-the-counter (OTC) use.

Jul 7, 2011Z-0119-2012—terminated

The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad.

Jul 7, 2011Z-0121-2012—terminated

The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad.

Jul 7, 2011Z-0123-2012—terminated

The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad.

Jul 7, 2011Z-0120-2012—terminated

The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad.

Jul 7, 2011Z-0122-2012—terminated

The first aid kits are recalled because the kits contain Iodine Prep Pad single use wipes which were recalled by Triad.