INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM, model no. NM-400L-0621 - 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.
Reported: February 17, 2021 Initiated: January 4, 2021 #Z-1010-2021
Product Description
INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM, model no. NM-400L-0621 - 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.
Details
- Recalling Firm
- Aomori Olympus Co., Ltd.
- Units Affected
- 7,400,000 (globally); 260,395 (US)
- Distribution
- US Nationwide distribution.
- Location
- Kuroishi, N/A
Frequently Asked Questions
What product was recalled? ▼
INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM, model no. NM-400L-0621 - 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.. Recalled by Aomori Olympus Co., Ltd.. Units affected: 7,400,000 (globally); 260,395 (US).
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 17, 2021. Severity: Moderate. Recall number: Z-1010-2021.
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