Home › Device types › BSP
Needle, Conduction, Anesthetic (W/Wo Introducer)
FDA product code BSP · Class 2 · Anesthesiology
3,139
Registered devices
1,308
Adverse events
17
Recalls
152
510(k) clearances
Devices with this code
EchoStim MSK — HAKKO CO.,LTD.PROBLOC* II Insulated Regional Block Needle — Avanos Medical, Inc.AVANOS — Avanos Medical, Inc.AccuTip — CLINT PHARMACEUTICALS, INC.Halyard — Avanos Medical, Inc.MSK Ultrasonic Injection Needle — Spectra Medical Devices, LLCMetal Standard Hub Tuohy Epidural Needle — Spectra Medical Devices, LLCPerifix® — B. BRAUN MEDICAL INC.TUOHY — Pajunk GmbH MedizintechnologiePhoenix — DR.JAPAN CO., LTD.Halyard — Avanos Medical, Inc.ARROW — TELEFLEX INCORPORATEDSONOTAP — Pajunk GmbH MedizintechnologieSPROTTE® NRFit — Pajunk GmbH MedizintechnologieEpimed — EPIMED INTERNATIONAL, INCAVANOS — Avanos Medical, Inc.Phoenix — DR.JAPAN CO., LTD.Phoenix — DR.JAPAN CO., LTD.Epimed — EPIMED INTERNATIONAL, INCAVANOS — Avanos Medical, Inc.VYGON — VYGONHalyard — Avanos Medical, Inc.SonoTAP® — Pajunk GmbH MedizintechnologieBD Quincke Spinal NRFit — BECTON, DICKINSON AND COMPANY
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-21 | ARROW INTERNATIONAL, LLC | Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss |
| 2020-12-08 | Smiths Medical ASD Inc. | The labeling was missing information on sterilization and prohibition of reuse. |
| 2019-12-20 | Arrow International Inc | Product lidstock contains the incorrect expiration date for the product |
| 2019-10-11 | TELEFLEX MEDICAL INC | Teleflex received the attached Medical Device Recall Notice from Pajunk Medical. Teleflex Medical is a distributor of Pajunk products. According to the notice, |
| 2019-10-11 | TELEFLEX MEDICAL INC | Teleflex received the attached Medical Device Recall Notice from Pajunk Medical. Teleflex Medical is a distributor of Pajunk products. According to the notice, |
| 2019-08-30 | Pajunk GmbH | Problem with packaging sealing process which affects sterility. |
| 2016-04-22 | Epimed International, Inc. | There is a possibility that the needles may have the potential to skive a catheters outer coating. If this were to occur, there exists the risk that a portion |
| 2015-05-01 | Integra LifeSciences Corp. d.b.a. Integra Pain Management | Integra LifeSciences Corp. d.b.a. Integra Pain Management Announces Voluntary Recall of Tuohy Needles (20 Gauge, 5 inch) due to incorrect packaging (labeled as |
| 2015-03-30 | Integra LifeSciences Corp. d.b.a. Integra Pain Management | A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged and labeled as 18 Gauge, 5 inch needles. |
| 2014-04-03 | B. Braun Medical, Inc. | B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte Needles that are missing the accompanying introducer needles. |
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