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NORTH AMERICAN RESCUE, LLC.

US

Last updated September 17, 2026

Information

Country
US
Address
35 TEDWALL COURT, Greer, SC, 29650
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3005034064
DUNS Number
—

Catalogue (3581)

Page 58 of 72
DeviceModel / ReferenceRegistriesClassStatus
NAR Kit 85-0916
FDA UDI
N/AUnknown
Nar 85-1973
FDA UDI
N/AActive
Nar 80-0857
FDA UDI
N/AActive
Nar 85-1719
FDA UDI
N/AActive
Nar 85-4473
FDA UDI
Class IActive
Nar 85-4183
FDA UDI
Class IActive
NAR Kit 85-1963
FDA UDI
N/AActive
Nar 80-1845
FDA UDI
Class IActive
NAR Kit 80-1175
FDA UDI
N/AActive
Nar 85-3429
FDA UDI
N/AActive
Nar 85-4684
FDA UDI
Class IActive
Nar 85-4005
FDA UDI
N/AActive
Nar 85-4228
FDA UDI
Class IActive
Nar 85-1979
FDA UDI
N/AActive
NAR Kit 85-0787
FDA UDI
N/AActive
Nar 80-1829
FDA UDI
NActive
Nar 85-2227
FDA UDI
N/AActive
NAR Kit 85-1253
FDA UDI
N/AActive
NAR Kit 80-0277
FDA UDI
N/AUnknown
NAR Kit 80-0308
FDA UDI
N/AActive
NAR Kit 85-1081
FDA UDI
N/AActive
Nar 85-1881
FDA UDI
N/AActive
Nar 85-0944
FDA UDI
Class IActive
Nar 84-0176
FDA UDI
Class IActive
Nar 80-1551
FDA UDI
Class IActive
Nar 85-4520
FDA UDI
Class IActive
Nar 85-1565
FDA UDI
N/AActive
Nar 85-2968
FDA UDI
N/AActive
NAR Kit 85-2098
FDA UDI
N/AActive
Nar 85-2996
FDA UDI
N/AActive
Nar 85-1716
FDA UDI
N/AActive
Nar 85-2480
FDA UDI
N/AActive
Nar 82-0063
FDA UDI
Class IActive
Nar 80-1212
FDA UDI
N/AActive
Nar 80-0859
FDA UDI
N/AActive
Nar 85-1045
FDA UDI
N/AActive
Nar 85-2523
FDA UDI
N/AActive
Nar 85-4943
FDA UDI
Class IActive
NAR Kit 80-0397
FDA UDI
N/AActive
Nar 85-4472
FDA UDI
Class IActive
NAR Kit 85-2768
FDA UDI
N/AActive
NAR Kit 80-0292
FDA UDI
N/AUnknown
Nar 85-2428
FDA UDI
N/AActive
Nar 85-4570
FDA UDI
NActive
NAR Kit 80-0038
FDA UDI
N/AActive
Nar 85-4117
FDA UDI
N/AActive
Nar 77-0082
FDA UDI
Class IActive
NAR Kit 85-3075
FDA UDI
N/AActive
Nar 85-1600
FDA UDI
N/AActive
NAR Kit 85-3029
FDA UDI
N/AActive

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FDA Recalls (4)

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
Mar 27, 2026Z-1947-2026—open, classified

Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the meter displays an E-5 error code for a very high blood glucose event (> 600 mg/dL) or when there is a test strip error, which can lead to operator confusion when evaluating patients and a delay in appropriate treatment. This is a downstream recall of Trividia Health Class I, Recall Event ID 98317.

Jul 1, 2025Z-2637-2025—open, classified

Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.

Aug 27, 2021Z-2520-2021—terminated

The device includes the incorrect Instructions for Use.

Aug 21, 2020Z-3018-2020—terminated

Lack of sterility assurance of the 30-0171