Walgreens 676988Recalls & reported problems

Summary

The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 00311917025278), received between Mar 13, 2018 and Jun 11, 2024 — classified as 14 malfunctions.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (7 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 16, 2026.

Most reported problems

Recent adverse event reports

The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 11, 2024Off-Label Use; Device Contamination with Chemical or Other Material; Off-Label Use; Device Contamination with Chemical or Other Material

  PET OWNER REPORTED PUSHING CLEAR LIQUID FROM THE BARREL ONTO THE NEEDLE PRIOR TO INJECTION. STATED, DOES NOT USE THE SYRINGES WITH CLEAR LIQUID. LOT: 2234067. CATALOG: 928855. DATE OF EVENT: UNKNOWN. SAMPLES: YES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19513822 ↗
• MalfunctionJul 15, 2022Separation Problem; Separation Problem

  IT WAS REPORTED THAT WHILE USING THE BD INSULIN SYRINGE (0.3ML) THE NEEDLE HUB SEPARATED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED WHEN HE REMOVED NEEDLE SHIELD, NEEDLE HUB SEPARATED. STATED, HE HAS TO TAKE MORE THAN 1 SYRINGE WHEN HE'S AWAY FROM HIS HOME BECAUSE HE'S CONCERNED THE ISSUE COULD HAPPEN AGAIN. LOT: 1165840, CATALOG: 928855, DATE OF EVENT: UNKNOWN, SAMPLES: YES . CL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15033980 ↗
• MalfunctionApr 20, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT 2 BOXES OF SYRINGE 0.3ML 30GA 8MM 10BAG 500 PL/WG HAD MISSING LABEL INFORMATION BEFORE USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: IT WAS REPORTED THAT THE EXPIRATION DATES WERE NOT ON THE BOX. A SECOND (B)(4) WAS CREATED TO CAPTURE MAT#928852 WITH LOT#5229810. VERBATIM: PHARMACY CALLING WITH 2 BOXES WALGREENS SYRINGE NOTED THE EXP DATES NOT ON THE BOX. PHARMACY REPORTED FOUND FULL BOX OF WALGREENS INSULIN SYRINGE 30G, 0.3ML 8MM WITH LOT # 6347590. LOT # 6347590. CATALOG# 928855. DATE OF EVENT (B)(6) 2021. SAMPLE NO. PHARMACY REPORTED FOUND FULL BOX OF WALGREENS INSULIN SYRINGE WITHOUT EXP DATES."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11692924 ↗
• MalfunctionFeb 18, 2021Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT A SYRINGE 0.3ML 30GA 8MM 10BAG 500 PL/WG SEPARATED FROM THE HUB DURING USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "IT WAS REPORTED THAT NEEDLE HUB SEPARATED INTO SHIELD. VERBATIM: CONSUMER REPORTED FOUND 1 ADDITIONAL SYRINGE ON (B)(6) 2021 FROM THIS BOX NEEDLE STUCK IN SHIELD"

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient

  MAUDE report 11346083 ↗
• MalfunctionNov 24, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 0.3ML 30GA 8MM 10BAG 500 PL/WG WAS MISSING LABEL INFORMATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 928855 BATCH, NO: 1116423. IT WAS REPORTED THAT THE BAG OF SYRINGES DID NOT HAVE A DATE ON THE BAG. VERBATIM: CONSUMER REPORTED FOUND 10 PACK OF WALGREEN SYRINGES. WAS ASKING IF THEY EXPIRE - DID NOT SEE A DATE ON BAG. OBTAINED THE LOT # AND DETERMINED THIS PRODUCT WAS EXPIRED. SHE DID NOT USE THIS ITEM IN YEARS.

  Patient problems: No Patient Involvement

  MAUDE report 10889709 ↗
• MalfunctionJul 7, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 0.3ML 30GA 8MM 10BAG 500 PL/WG WAS MISSING LABEL INFORMATION. THIS WAS DISCOVERED BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 928855 BATCH NO: 9203941. IT WAS REPORTED BOXES DID NOT HAVE EXP DATES ON THEM.

  Patient problems: No Patient Involvement

  MAUDE report 10243245 ↗
• MalfunctionJun 8, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT DURING USE THE HUB SEPARATED FROM DEVICE AND STUCK IN SHIELD WITH A BD SYRINGE 0.3ML 30GA 8MM. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED FOUND SEVERAL NEEDLE HUB ASSEMBLY STUCK IN SHIELD.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10130924 ↗
• MalfunctionJun 5, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 0.3ML 30GA 8MM 10BAG 500 PL/WG WAS MISSING LABEL INFORMATION. THIS WAS DISCOVERED BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 928855 BATCH NO. 8121963 IT WAS REPORTED THAT EXPIRATION DATE WAS NOT ON THE BOX.

  Patient problems: No Patient Involvement

  MAUDE report 10125924 ↗
• MalfunctionMay 8, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED BEFORE USE THE SYRINGE 0.3ML 30GA 8MM 10BAG 500 PL/WG HAD NO LABEL OR MISSING LABEL INFORMATION OR ILLEGIBLE (ALL PACKAGING LEVELS). THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PHARMACIST CALLED TO GET ASSISTANCE WITH LOCATING EXPIRATION DATE ON BOX, STATED HE ONLY HAD A LOT NUMBER. THE BOX OF PRODUCT WAS MISSING EXPIRATION DATE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10039287 ↗
• MalfunctionDec 31, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT BD¿ INSULIN SYRINGE CAME WITH A MIX OF PRODUCT TYPES. THIS WAS DISCOVERED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 928855 BATCH NO. 7261532 IT WAS REPORTED THAT A SHELF CARTON CONTAINED MIXED PRODUCT. OUT OF 10 BAGS IN THE SHELF CARTON, 9 WERE 0.3ML AND ONE WAS 0.5ML. VERBATIM: ISSUE: CONSUMER REPORTED OUT OF 10 BAGS IN THE BOX OF OF 3/10 ML, 30G, 8MM SYRINGES SHE FOUND 1 BAG WAS A BAG OF OF .5ML. 30G, 8MM SYRINGES. SHE DID NOT USE THESE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9534211 ↗
• MalfunctionMar 4, 2019Leak/Splash; Device Contamination with Chemical or Other Material; Leak/Splash; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT BD¿ INSULIN SYRINGE HAD FLUID IN THE SYRINGES AND THE SYRINGES LEAKED. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED. VERBATIM: "MATERIAL NO.: 928855, BATCH NO.: 8121963. IT WAS REPORTED BY THE CONSUMER THAT THERE WAS FLUID IN THE SYRINGES AND THE SYRINGES LEAKED. VERBATIM: CONSUMER REPORTED FLUID IN SYRINGES, STATED THAT THE SYRINGES LEAKED. CONSUMER PROVIDED LOT # 8121963, 30G, 3/10ML, 8MM (PRODUCT # 928855). SHE WOULD NOT PROVIDE ANY ADDITIONAL INFORMATION, STATED THAT HER ATTORNEY ADVISED HER NOT TO GIVE ANY INFORMATION. SHE CALLED FOR MAILING ADDRESS TO SEND SYRINGES FOR TESTING. I ADVISED HER TO HAVE HER ATTORNEY CONTACT US."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8387972 ↗
• MalfunctionOct 29, 2018Leak/Splash; Contamination /Decontamination Problem

  IT WAS REPORTED THAT BEFORE USE OF THE BD¿ INSULIN SYRINGE A CLEAR LIQUID WAS NOTICED INSIDE THE BARREL OF THE SYRINGE. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8015602 ↗
• MalfunctionAug 30, 2018Device Markings/Labelling Problem

  IT WAS REPORTED THAT BD¿ INSULIN SYRINGE HAD SMEARED SCALE MARKING ON THE SYRINGE BARREL. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7834710 ↗
• MalfunctionMar 13, 2018Crack; Leak/Splash

  IT WAS REPORTED THAT A BD¿ INSULIN SYRINGE WAS CRACKED ON ONE SIDE AND LEAKED WHEN DRAWING UP INSULIN. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTIONS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7334935 ↗