CLASS II Drug recall · Reported 14 Dec 2016 · FDA Enforcement Report
K-9 Trauma Field Kit recalled by North American Rescue
North American Rescue is recalling K-9 Trauma Field Kit, distributed nationwide in the US. The recall was initiated on 27 Sep 2016 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0179-2017
- FDA event ID
- 75415
- Recalling firm
- North American Rescue, Greer, SC
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 27 Sep 2016
- FDA classified
- 8 Dec 2016
- Reported
- 14 Dec 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Sterility
Timeline
| 27 Sep 2016 | Recall initiated by company | |
| 8 Dec 2016 | Classified by FDA | +72 days |
| 14 Dec 2016 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue
Where it was distributed
Nationwide, Australia & Switzerland
Questions about this recall
Why was it recalled?
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Which lots are affected?
Kit Part # 80-0211 - Kit Lot # 80-0211070616, 80-0211051316, 80-0211041816, 80-0211030216, 80-0211072216, 80-0210070716, 80-0210050416W, 80-0210072216; Kit Part # 80-0304 - Kit Lot # 80-0304041916; Kit Part # 80-0209 - Kit Lot # 80-0209082216, 80-0209051816, 80-0209051616, 80-029050316, 80-0209041916, 80-0209060316; Kit Part # 80-210 Kit Lot # 80-021007076, 80-0210050416W, 80-0210072216; Kit Part # 80-0300 - Kit Lot # 80-0300081216, 80-0300050916, 80-0300050316, 80-0300041916, 80-0300082416; Kit Part #80-0301 - Kit Lot # 80-0301042916, 80-0301050316
Where was it sold?
Nationwide, Australia & Switzerland
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
8 other products · FDA event 75415This product is part of a recall event; the main page for the event is Advance Trauma Kit recalled by North American Rescue.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Advance Trauma Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | Range Trauma Kit Hardcase recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | Range Trauma Kit ORG recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | USCG Boat Response Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | Aid Backpack Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | Mini Resupply Trauma Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | Range Trauma Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide | |
| CLASS II | Amphibious Trauma Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide |
More recalls from North American Rescue
All 13| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | AIDBAGs are first aid kits of convenience composed recalled | North American Rescue | Device Malfunction | CA, WA |
| Device | CLASS II | Junctional Emergency Treatment Tool (jett) recalled | North American Rescue | Device Malfunction | Nationwide |
| Device | CLASS II | ARS Decompression Needle recalled by North American Rescue | North American Rescue | Other | PR |
| Device | CLASS II | Flat Responder Emergency Trauma Dressing recalled | North American Rescue | Sterility | Nationwide |
| Drug | CLASS II | Amphibious Trauma Kit recalled by North American Rescue | North American Rescue | Sterility | Nationwide |