BD 1mL TB Syringe Slip Tip 309625Recalls & reported problems

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 00382903096251), received between Apr 16, 2018 and May 17, 2023 — classified as 11 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (6 reports).

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 17, 2023Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT THE BD SLIP TIP¿ SYRINGE WITH BD SAFETYGLIDE¿ SAFETY NEEDLE EXPERIENCED FOREIGN MATTER ON THE NEEDLE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CLUMP OF WHITE HARD MATTER ON NEEDLE. TYPE OF INCIDENT/PROBLEM: DEFECT (DETECTED BEFORE USE). LEVEL OF HARM: NO EFFECT - DID NOT REACH PATIENT - DETECTED BEFORE USE OR DOES NOT TOUCH PERSON DURING USE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16950696 ↗
• MalfunctionApr 25, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT PRIOR TO USING THE 1 ML BD SLIP TIP SYRINGE WITH ATTACHED NEEDLE 26 G X 3/8 IN., THAT NEEDLE HUB COMES OFF WITH SHIELD REMOVAL. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: STATED THAT WHEN HE TRIES TO REMOVE THE SHIELD THE NEEDLE HUB COMES OFF WITH IT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14196932 ↗
• MalfunctionAug 17, 2021Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE NEEDLE HUB SEPARATED FROM THE SYRINGE 1ML S/T W/NDL 26X3/8 IB WHEN REMOVING THE SHIELD. THIS OCCURRED WITH 6 SYRINGES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CONSUMER REPORTED, WHEN HE REMOVES NEEDLE SHIELD, NEEDLE HUB SEPARATES".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12331826 ↗
• MalfunctionMar 10, 2021Volume Accuracy Problem; Volume Accuracy Problem

  IT WAS REPORTED THAT THE SYRINGE 1ML S/T W/NDL 26X3/8 IB HAD NO SCALE MARKINGS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE GRADUATION ON THE SYRINGE DISAPPEAR."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11452936 ↗
• MalfunctionSep 1, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT SYRINGE 1ML S/T W/NDL 26X3/8 IB HAD THE NEEDLE AND SYRINGE SPIN OUT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT WAS REPORTED WHEN REMOVING THE SHIELD THE NEEDLE GOES WITH IT. VERBATIM: CONSUMER REPORTED WHEN REMOVING THE SHIELD THE NEEDLE GOES WITH IT. INFORMED TO SEAT THE NEEDLE STILL SEEING THIS ISSUE. CALLER GETS 12 SYRINGES AT A TIME. LOT #: 8327216, CATALOG#: 309625, DATE OF EVENT: 08/10/2020, SAMPLES STATUS AWAITING SAMPLE:"

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10475383 ↗
• MalfunctionAug 17, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT AN UNSPECIFIED NUMBER OF BD 1ML TUBERCULIN SYRINGE SLIP TIPS W / DETACHABLE NEEDLES EXPERIENCED THE NEEDLE AND SYRINGE SEPARATING / SPINNING OUT DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 309625, BATCH NO: 9353360. IT WAS REPORTED THAT WHEN RN IS ADMINISTERING AN IMMUNOTHERAPY INJECTION, THE NEEDLE REMAINS IN THE PATIENT AND THE PATIENT DOES NOT RECEIVE THE APPROPRIATE DOSE ORDERED. AFTER DISCUSSING THIS WITH MANAGEMENT, WE FELT THAT IT WASN'T NECESSARY TO SEND SAMPLES IN FOR INVESTIGATION. AS PREVIOUSLY MENTIONED, THE MORE WE LOOKED INTO THIS ISSUE, WE REALIZED WE COULD HAVE BEEN USING THE NEEDLES WITH A MORE COMPATIBLE LUER LOCK STYLE SYRINGE. MOVING FORWARD WE WOULD LIKE TO IMPLEMENT THIS, AND EXPECT THAT USING THE LUER LOCK SYRINGE WOULD PREVENT ANY FURTHER MALFUNCTIONS. I BELIEVE IT HAS OCCURRED APPROXIMATELY 4 TIMES. TWICE THIS MONTH ON (B)(6) 2020 FOR TWO DIFFERENT RN'S. LOT#: 9361589, REF#: 305758 FOR NEEDLE. LOT#: 9353360, REF#: 309625 FOR SYRINGE. AS I MENTIONED IN THE PREVIOUS EMAIL, UPON FURTHER INVESTIGATION, WE BELIEVE THIS OCCURRED BECAUSE WE OF THE TYPE OF SYRINGE WE WERE USING. IF YOU WOULD STILL LI

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10418381 ↗
• MalfunctionAug 14, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT SYRINGE 1ML S/T W/NDL 26X3/8 IB HAD CONNECTIVITY ISSUES. THIS WAS DISCOVERED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 309625, BATCH NO: 9353360. IT WAS REPORTED THAT WHEN RN IS ADMINISTERING AN IMMUNOTHERAPY INJECTION, THE NEEDLE REMAINS IN THE PATIENT AND THE PATIENT DOES NOT RECEIVE THE APPROPRIATE DOSE ORDERED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10411650 ↗
• MalfunctionDec 18, 2018Leak/Splash

  IT WAS REPORTED THAT A 1 ML BD¿ SLIP TIP SYRINGE WITH ATTACHED NEEDLE LEAKED AT THE NEEDLE DURING ASPIRATION OF INSULIN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8174761 ↗
• MalfunctionJul 25, 2018Material Separation

  IT WAS REPORTED THAT BD¿ SLIP TIP SYRINGE HAD NEEDLE SEPARATION. THERE WAS NO REPORT OF EXPOSURE, SERIOUS INJURY OR MEDICAL INTERVENTION.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7718701 ↗
• MalfunctionMay 30, 2018Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT FOREIGN MATTER (DESCRIBED AS ¿PLASTIC SHARDS¿) WERE FOUND IN MULTIPLE BD¿ SLIP TIP SYRINGE(S) WITH NEEDLE. THERE WAS NO REPORT OF EXPOSURE, INJURY OR MEDICAL INTERVENTION.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7554220 ↗
• MalfunctionApr 16, 2018Leak/Splash

  IT WAS REPORTED THAT A BD¿ SLIP TIP SYRINGE WITH ATTACHED NEEDLE (INTRADERMAL BEVEL, STERILE, SINGLE USE) LEAKED DURING USE. THERE WAS NO REPORT OF EXPOSURE, INJURY OR MEDICAL INTERVENTIONS.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7434368 ↗