Aomori Olympus Co., Ltd. Recall: INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM, model no. NM-400L-0
Aomori Olympus Co., Ltd. Recall: INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM, model no. NM-400L-0 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Aomori Olympus Co., Ltd.; Product: INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM, model no. NM-400L-0625 - Product Usage: Used with endoscopes to perform en
| Recalling firm | Aomori Olympus Co., Ltd. |
|---|---|
| Product | INJECTOR FORCEMAX UP 2.8MMCH 25G 6MM, model no. NM-400L-0625 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract. |
| Reason for recall | Inspection confirmed a small percentage of sterile packages with inadequate package seal (partial heat seal). Patients may develop infections if non-sterile equipment is used. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | US Nationwide distribution. |
| Recall initiated | 20210104 |
| Recall number | Z-1000-2021 |
| Category | device |
| State | N/A |
| Country | Japan |
$29/mo
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