Injection needle 50-345-23Recalls & reported problems
Spiggle & Theis Medizintechnik GmbH · curved, luer-lock wl 24 cm, total length 31 cm · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jun 27, 2025Open, Classified
Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.
Z-2331-2025 · Root cause: Under Investigation by firm · FDA record ↗
Other NEEDLE, ASPIRATION AND INJECTION, REUSABLE devices
- Injection needle 50-353-23Spiggle & Theis Medizintechnik GmbH · NEEDLE, ASPIRATION AND INJECTION, REUSABLE1 recall0 reports
- ASPIRATION NEEDLE NA-1C-1Olympus Medical Systems Corp. · NEEDLE, ASPIRATION AND INJECTION, REUSABLE1 death5 reports
- Breast Localization Needles 252125Argon Medical Devices, Inc. · Needle, Aspiration And Injection, Reusable2 reports
- Breast Localization Needles 253050Argon Medical Devices, Inc. · Needle, Aspiration And Injection, Reusable2 reports
- Breast Localization Needles 252100Argon Medical Devices, Inc. · Needle, Aspiration And Injection, Reusable1 report
- Breast Localization Needles 253125Argon Medical Devices, Inc. · Needle, Aspiration And Injection, Reusable1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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