BD IntegraRecalls & reported problems across all models

We found 12 models of BD Integra by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 630 adverse event reports in the FDA's MAUDE database, received between Jan 19, 2017 and Aug 14, 2026 — classified as 93 injuries, 537 malfunctions.

The most frequently reported specific device problem is “Leak/Splash” (255 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported BD Integra problems

BD Integra models

12 models, most reported first. Each model has its own page with its reports, recalls and device details.

• BD Integra 305270

  SYRINGE, ANTISTICK
  261 reports
• BD Integra 305271

  SYRINGE, ANTISTICK
  106 reports
• BD Integra 305269

  SYRINGE, ANTISTICK
  85 reports
• BD Integra 305272

  SYRINGE, ANTISTICK
  71 reports
• BD Integra 305274

  SYRINGE, ANTISTICK
  45 reports
• BD Integra 305283

  SYRINGE, ANTISTICK
  21 reports
• BD Integra 305311

  SYRINGE, ANTISTICK
  16 reports
• BD Integra 305310

  SYRINGE, ANTISTICK
  11 reports
• BD Integra 305273

  SYRINGE, ANTISTICK
  5 reports
• BD Integra 305313

  SYRINGE, ANTISTICK
  5 reports
• BD Integra 305275

  SYRINGE, ANTISTICK
  2 reports
• BD Integra 305312

  SYRINGE, ANTISTICK
  2 reports

Recent BD Integra adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionAug 14, 2026Leak/Splash

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50246537 ↗
• MalfunctionAug 14, 2026Leak/Splash

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50246532 ↗
• MalfunctionMar 12, 2026Leak/Splash

  NO ADDITIONAL INFORMATION.

  Patient problems: Insufficient Information

  MAUDE report 24586483 ↗
• MalfunctionFeb 26, 2026Leak/Splash

  IT WAS REPORTED THAT BD SYRINGE INTEGRA 3ML W/NDL 25X1 RB CAUSED LEAKAGE. RCC RECEIVED A COMPLAINT VIA EMAIL. I JUST USED A BD INTEGRA SYRINGE 3ML 25G 1" TW (0.5MM X 25MM) FOR CYANOCOBALAMIN (B-12) INJECTION INTO MY THIGH, WHICH I DO MONTHLY. I HAVE BEEN ON B-12 SINCE THE 1990S. AS I FULLY PUSHED IT IN, THIS SYRINGE LEAKED BETWEEN THE UPPER PART (NEEDLE) AND THE LOWER PART (VIAL), SPILLING ONTO MY HAND AND THE CARPET. I HAVE NO IDEA HOW MUCH I WENT INTO MY MUSCLE. MAYBE NOTHING! I TRIED TO SCAN THE QR CODE BUT WAS UNABLE. (B)(4), LOT 4304388. CRACK: NOT THAT I CAN SEE LOOSE CONNECTION: I'M NOT SURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24455574 ↗
• MalfunctionJan 22, 2026Break

  NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24153921 ↗
• MalfunctionJan 22, 2026Break

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML W/NDL 25X1 RB NEEDLE WAS BROKEN, THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305270 BATCH#: 2244656. RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. CUSTOMER STATES THAT HE IS USING THE INTEGRA SYRINGE AND 3 NEEDLES BROKE OFF AND ARE IN HIS LEG. CUSTOMER SAID THAT HIS DOCTOR SAID HE WOULD HAVE TO HAVE SURGERY TO REMOVE THEM. CUSTOMER HAS PRODUCT TO RETURN IF NEEDED FOR INVESTIGATION. REF#: 305270 LOT#: 2244656 ADDITIONAL INFO RECEIVED: IT WAS 3 SEPARATE INSTANCES OVER THE LAST MONTH. THE LAST ONE WAS ON DEC 27. I HAVE BEEN GIVING MYSELF SHOTS SINCE 2017-2018 WITHOUT A PROBLEM. I GOT THESE SYRINGES AND THE PROBLEMS BEGAN. I NOW HAVE 3 NEEDLES STUCK IN MY MUSCLE. CAN YOU CONFIRM IF AN X RAY WAS DONE TO CHECK FOR A NEEDLE IN THE LEG? HAS THERE BEEN ANY MEDICAL INTERVENTION SO FAR? ANY PAIN MEDICATIONS? ANY SWELLING AT INJECTION SITE OR CURRENT SIGNS OF INFECTION? ANY SURGERY DATE SCHEDULED? NONE. I FOUND OUT 2 DAYS AGO THE SYRINGE RETRACTS THE NEEDLE, SO I DO NOT BELIEVE THERE ARE NEEDLES IN MY LEG.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24153620 ↗
• InjuryDec 14, 2025Break; Break

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML W/NDL 25X1 RB NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL: 305270; BATCH#: 2080949. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. I USED A BD INTEGRA SYRINGE TO INJECT A PRESCRIBED HORMONE REPLACEMENT. I HAVE USED THEM SUCCESSFULLY FOR A COUPLE OF YEARS WITHOUT ANY ISSUES UNTIL YESTERDAY. I INJECTED MY HORMONE REPLACEMENT, AND THE NEEDLE DISCONNECTED FROM THE SYRINGE AND SHOT INTO MY LEG. THIS CAUSED A TRIP TO THE EMERGENCY ROOM, AND A CONSULTATION WITH A SURGEON WHO SAID THE NEEDLE IS EMBEDDED TOO DEEP IT THE LEG MUSCLE, TENDONS, NERVES, THAT HE FELT FOR NOW, THE SURGERY TO REMOVE IT WOULD CAUSE MORE HARM AND DAMAGE THEN JUST LEAVING IT IN. IN THE FUTURE A SURGERY MAY BE REQUIRED IF THE NEEDLE CAUSES ANY FURTHER PAIN OR DAMAGE TO THE LEG. I AM EXTREMELY UPSET BY THIS SITUATION, AS I HAVE BEEN USING THESE NEEDLES TO INJECT MY HORMONE REPLACEMENT FOR MANY YEARS WITHOUT INCIDENT. I HAVE INCURRED DISTRESS AND FINANCIAL LOSS DUE TO THIS SITUATION, AND MAY NEED A SURGERY ON THE FUTURE TO REMOVE IT. I AM REQUESTING RESPONSE REGARDING THE ACTIONS THAT BD INTEGRA WILL TAKE TO ENSURE T

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 23799584 ↗
• MalfunctionOct 16, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML W/NDL 25X1 RB HAD LEAKAGE PAST THE STOPPER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305270. BATCH#: 2206535. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. RN WAS ADMINISTERING DECITABINE INTO RIGHT LOWER ABDOMEN. NEEDLE INSERTED THROUGH SKIN, AND PLUNGER DEPRESSED. ONCE RN PRESSED DOWN ON PLUNGER, LIQUID BEGAN TO SPILL FROM THE PLUNGER. NEEDLE RETRACTED AND PLACED ON TABLE WHERE CHEMO SPILLED ON THE TABLE. APPROXIMATELY, THREE DROPS OF CHEMO GOT ON PATIENT'S PANTS (DRIED UP WITH GAUZE.) PT INSTRUCTED TO WASH PANTS ON WITH HOT WATER/HIGH HEAT AND DRY PANTS ON HIGH HEAT. ITEM# 305270. BATCH# 2206535.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23319723 ↗
• MalfunctionOct 15, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML LL W/NDL 25X5/8 RB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305269 BATCH#: 2307009. RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. CUSTOMER STATES THAT WHEN THEY WENT TO GIVE 2 PATIENTS MEDICATION, THE MEDICATION SHOT OUT THE SIDE WHERE THE NEEDLE CONNECTS TO THE SYRINGE. BOTH INSTANCES HAPPENED TODAY 23SEP2025. PATIENTS HAD TO BE RE-ADMINISTERED MEDICATION SINCE THEY DID NOT RECEIVE IT THE FIRST TIME. REF#: 305269 LOT #: 2307009. CUSTOMER HAS PRODUCT TO RETURN IF NEEDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23285602 ↗
• MalfunctionOct 15, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML LL W/NDL 25X5/8 RB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305269 BATCH#: 2307009. RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. CUSTOMER STATES THAT WHEN THEY WENT TO GIVE 2 PATIENTS MEDICATION, THE MEDICATION SHOT OUT THE SIDE WHERE THE NEEDLE CONNECTS TO THE SYRINGE. BOTH INSTANCES HAPPENED TODAY (B)(6) 2025. PATIENTS HAD TO BE RE-ADMINISTERED MEDICATION SINCE THEY DID NOT RECEIVE IT THE FIRST TIME. REF#: 305269, LOT #: 2307009. CUSTOMER HAS PRODUCT TO RETURN IF NEEDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23285189 ↗
• MalfunctionJul 21, 2025Break; Break

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML W/NDL 23X1 RB NEEDLE WAS BROKEN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305271, LOT#: 2271484. RCC RECEIVED A COMPLAINT VIA EMAIL. ON SATURDAY JULY 5TH, WE RECEIVED A PRODUCT COMPLAINT VIA XXX DIRECT MESSAGE FROM A USER NAMED XXXX REGARDING A DEFECT WHILE USING A BD INTEGRA SYRINGE. ATTACHED IS A PHOTO OF THE USER¿S DIRECT MESSAGE AND PHOTOS OF THE SYRINGE¿S PACKAGING INCLUDING THE LOT NUMBER. PLEASE NOTE THAT WE HAVE RESPONDED TO THIS PERSON WITH OUR STANDARD REPLY ASKING THEM TO CONTACT THE PRODUCT COMPLAINTS TEAM BY EMAIL OR PHONE. PRODUCT#: 305271, LOT#: 2271484. HEY THERE. I'M NOT SURE IF YOU'VE HAD ANY OTHER COMPLAINTS, BUT I WANTED TO SEND A MESSAGE ABOUT THIS NEEDLE. I WAS GIVEN MY HUSBAND HIS SHOT TONIGHT, AND THIS IS THE FIRST SYRINGE/NEEDLE WE HAD GOTTEN FROM THIS BRAND. AND WHILE I WAS GIVING HIM SHOT, THE NEEDLE BROKEN OFF WHILE IN HIS SKIN. I WAS ABLE TO PULL IT STRAIGHT OUT, SO IT STAYED ON. BUT I WALKED OVER TO THE SINK TO LOOK AND SEE IF IT DID BREAK, AND IT FELL OUT INTO MY KITCHEN SINK. ADDITIONAL INFORMATION PROVIDED: 1. CAN YOU PLEASE PROVIDE AN EXACT DATE OF EVENT IN THIS FORMA

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22561478 ↗
• MalfunctionJul 11, 2025Retraction Problem; Retraction Problem

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML LL W/NDL 25X5/8 RB NEEDLE RETRACTED PREMATURELY. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305269 BATCH#: 1270380. RCC RECEIVED A COMPLAINT VIA PHONE. PIR ATTACHED. PRODUCTCOMPLAINT REF 305269 LOT 1270380 ISSUE: RN WHILE INJECTING VACCINE SYRINGE RETRACTED WHILE THERE WAS STILL ADMINISTERING. PREMATURE RETRACTION. DOE 27JUNE2025. SECOND INCIDENT SAME PREMATURE RETRACTION, CUSTOMER SAID SAME LOT. DOE: 27MAY2025. ADDITIONAL INFO: ANY ADVERSE EVENT OR SERIOUS INJURY REPORTED TO PATIENT OR HEALTHCARE PROFESSIONAL? IF YES, PLEASE PROVIDE THE DETAILS. TOTAL NUMBER OF OCCURRENCES? 3 WHEN YOU PRESSED THE BUTTON, DID THE NEEDLE FULLY RETRACT? NO, THE NEEDLE RETRACTED DURING ADMINISTRATION. DID THE NEEDLE RETRACT SLOWER THAN NORMAL? NO, FASTER THAN NORMAL DID THE NEEDLE START RETRACTING AND THEN STOP, LEAVING THE NEEDLE EXPOSED ? YES, AND THIS TOOK PLACE DURING ADMINISTRATION DID THE NEEDLE NOT MOVE AT ALL AFTER PRESSING THE BUTTON? THE BUTTON WAS NOT PRESSED AT ALL DID THE BUTTON DEPRESS? NO

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22487645 ↗
• MalfunctionJul 11, 2025Retraction Problem; Retraction Problem

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML LL W/NDL 25X5/8 RB NEEDLE RETRACED PREMATURELY. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL#: 305269, BATCH#: 1270380. VERBATIM: RCC RECEIVED A COMPLAINT VIA PHONE. PRODUCTCOMPLAINT: REF 305269, LOT 1270380. ISSUE: RN WHILE INJECTING VACCINE SYRINGE RETRACTED WHILE THERE WAS STILL ADMINISTERING. PREMATURE RETRACTION. DOE (B)(6) 2025. SECOND INCIDENT SAME PREMATURE RETRACTION, CUSTOMER SAID SAME LOT. DOE: 27MAY2025. ADDITIONAL INFO: ANY ADVERSE EVENT OR SERIOUS INJURY REPORTED TO PATIENT OR HEALTHCARE PROFESSIONAL? IF YES, PLEASE PROVIDE THE DETAILS. TOTAL NUMBER OF OCCURRENCES? 3. WHEN YOU PRESSED THE BUTTON, DID THE NEEDLE FULLY RETRACT? NO, THE NEEDLE RETRACTED DURING ADMINISTRATION. DID THE NEEDLE RETRACT SLOWER THAN NORMAL? NO, FASTER THAN NORMAL. DID THE NEEDLE START RETRACTING AND THEN STOP, LEAVING THE NEEDLE EXPOSED ? YES, AND THIS TOOK PLACE DURING ADMINISTRATION. DID THE NEEDLE NOT MOVE AT ALL AFTER PRESSING THE BUTTON? THE BUTTON WAS NOT PRESSED AT ALL DID THE BUTTON DEPRESS? NO.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22487640 ↗
• InjuryJul 11, 2025Break; Break

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML W/NDL 25X1 RB NEEDLE PULLED OUT OF THE HUB. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER; MATERIAL#: 305270, BATCH#: 2356038. VERBATIM: CUSTOMER FILLED OUT AN ONLINE FORM. "ONE OF YOUR SYRINGES PUSHED A NEEDLE INTO MY HUSBAND'S ARM. I WOULD LIKE TO DISCUSS THIS." CUSTOMER RESPONSE: ON (B)(6) 2025, I GAVE MY HUSBAND AN INJECTION USING A BD INTEGRA SYRINGE (3 ML 25 G). INSTEAD OF THE PLUNGER STOPPING WHEN THE MEDICINE WAS OUT, THE PLUNGER CONTINUED UNTIL THE NEEDLE WAS INJECTED INTO MY HUSBAND'S ARM AND DISAPPEARED. HE WENT TO THE ER TO SEE WHAT COULD BE DONE. THEY CAUGHT A GLIMPSE OF IT USING AN ULTRASOUND BUT COULD NOT FIND IT ON AN X-RAY. NOW, WE HAVE A HOSPITAL BILL AND A NEEDLE FLOATING AROUND SOMEWHERE INSIDE MY HUSBAND. FROM HERE ON OUT, WE HAVE TO BE CONCERNED ABOUT THIS NEEDLE, ESPECIALLY IF AN MRI IS EVER IN THE PICTURE. SEBASTIAN WORKS A RATHER DANGEROUS JOB AND IF HE'S EVER HURT OR KNOCKED UNCONSCIOUS, WE HAVE TO BE SURE HE DOESN'T EVER HAVE AN MRI AS THE NEEDLE COULD COME OUT FROM ANYWHERE WHICH WOULD DAMAGE NOT ONLY THE MRI MACHINE BUT MY HUSBAND.

  Patient problems: Foreign Body In Patient

  MAUDE report 22480894 ↗
• MalfunctionMay 20, 2025Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE BD SYRINGE INTEGRA 3ML LL W/NDL 25X5/8 RB HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE SYRINGE/NEEDLE COMBINATION LEAKED. DISCOVERED BY: SITE NURSE. DATE OF DISCOVERY: (B)(6) 2025. DATE OF OCCURRENCE: (B)(6) 2025. ITEM NUMBER: 305269. LOT NUMBER: 0259746. WHEN THE STUDY DRUG WAS BEING ADMINISTERED, THE NURSE NOTICED SOME DROPS OF THE STUDY DRUG HAD LEAKED OUT. ADMINISTRATION WAS STOPPED AND THE NEEDLE/SYRINGE WAS ASSESSED. THE NEEDLE OF THE SYRINGE WAS REPLACED AND THE REMAINDER OF THE STUDY DRUG (0.7 ML) WAS ADMINISTERED WITHOUT ISSUE. THE TOTAL VOLUME OF STUDY DRUG AT THE BEGINNING WAS 1.6ML BUT IT IS UNCLEAR HOW MUCH HAD LEAKED; THEREFORE, IT IS UNKNOWN HOW MUCH OF THE STUDY DRUG WAS ADMINISTERED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22057107 ↗

Other Becton, Dickinson And Company products

• BD Vacutainer SST10 models · 4,985 reports · 3 recalls
• BD Luer-Lok48 models · 5,117 reports
• BD Insyte Autoguard33 models · 4,465 reports · 8 recalls
• BD SafetyGlide17 models · 2,185 reports
• BD Vacutainer Eclipse Blood Collection Needle4 models · 1,880 reports
• BD Vacutainer Push Button Blood Collection Set9 models · 1,831 reports
• BD Nexiva25 models · 1,614 reports · 1 recall
• BD BACTEC MGIT Mycobacteria Growth Indicator Tubes2 models · 1,554 reports