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Anrei

Anrei Medical(HZ) Co.,Ltd. · Model NE-C2508 · UDI-DI 06926839809147

FBK
1
510(k) clearances
570
Adverse events
42
Recalls
98
Facilities

Description

Single Use Injection Needle

Recalls

DateFirmReason
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2024-10-04Hobbs Medical, Inc.Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inne
2023-10-24Karl Storz EndoscopyThe efficacy of the manual cleaning process cannot be assured for the affected injection needles intended for general surgery and visceral surgery, which if used, may expose the pa

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.