Walgreens 676987Recalls & reported problems

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00311917025285), received between May 18, 2018 and Jul 18, 2024 — classified as 13 malfunctions.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (5 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 18, 2024Material Puncture/Hole; Material Puncture/Hole

  PHARMACIST REPORTED FOUND 1 SYRINGE WITH THE NEEDLE STICKING OUT THE NEEDLE SHIELD IN ONE 10 PACK THAT WAS SEALED. DISCARDED THE 10 PACKET. NO INJURY FROM THIS INCIDENT. DC LOT # 2115706 CATALOG# 928854 DATE OF EVENT UNKNOWN SAMPLE STATUS DISCARD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19779062 ↗
• MalfunctionDec 14, 2022Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED WHILE USING WALGREENS SUPER THIN II SYRINGES SHORT NEEDLE THE EXPIRATION DATE WAS MISSING. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PHARMACIST CALLED TO INQUIRE ABOUT EXPIRATION DATE ON SYRINGES. THERE IS NO EXPIRATION DATE ON THE BOX.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15983001 ↗
• MalfunctionJan 28, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT 3 BOXES OF SYRINGE 0.5ML 30GA 8MM 10BAG 500 PL/WG HAD MISSING LABEL INFORMATION DURING USE. THE FOLLOWING WAS REPORTED BY THE INITIAL REPORTER: "IT WAS REPORTED THAT EXPIRATION DATE IS MISSING FROM SHELF CARTON. (B)(4) RECORDS ISSUE IF MISSING EXPIRATION DATE FOR CAT 928853. (B)(4) RECORDS ISSUE IF MISSING EXPIRATION DATE FOR CAT 928854. VERBATIM: WALGREEN'S PHARMACIST STATED HE HAD 3 BOXES OF INSULIN SYRINGES WITHOUT EXPIRATION DATES. ADVISED THAT THE PRODUCT BOXES COULD BE EXPIRED.".

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement

  MAUDE report 11248608 ↗
• MalfunctionNov 3, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT SYRINGE 0.5ML 30GA 8MM 10BAG 500 PL/WG NEEDLE HUB SEPARATED ON 9 OCCASIONS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 928854 BATCH NO. 9324122. IT WAS REPORTED THAT 9 NEEDLE HUBS SEPARATED FROM SYRINGES.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10782885 ↗
• MalfunctionAug 5, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT PRIOR TO USE IT WAS DISCOVERED THAT THE EXPIRATION DATE WAS MISSING ON BOX WITH A BD SYRINGE 0.5ML 30GA 8MM. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PHARMACIST CALLED TO INQUIRE ABOUT EXPIRATION DATE ON (B)(6) SYRINGES. PHARMACIST STATED THAT THERE IS NO EXPIRATION DATE ON THE BOX.

  Patient problems: No Patient Involvement

  MAUDE report 10371180 ↗
• MalfunctionAug 4, 2020Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED DURING USE THE BD SYRINGE 0.5ML 30GA 8MM HAD FOREIGN MATTER ON THE DEVICE/CANNULA IN FLUID PATH. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE CONSUMER FOUND A SMALL AMOUNT OF LIQUID ON THE TIP OF HIS NEEDLE WHEN HE DEPRESSED THE PLUNGER ROD.

  Patient problems: No Patient Involvement

  MAUDE report 10365009 ↗
• MalfunctionJul 9, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT AN UNSPECIFIED NUMBER OF SYRINGES 0.5ML 30GA 8MM 10BAG 500 PL/WG EXPERIENCED MISSING LABEL INFORMATION WHICH WAS NOTED PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 928854 BATCH NO: 9176552. COMPLAINT 1 OF 3 PHARMACY REPORTED- 3 DIFFERENT BOXES DID NOT HAVE EXP DATES ON THEM. DATE OF EVENT: (B)(6) 2020.

  Patient problems: No Patient Involvement

  MAUDE report 10255803 ↗
• MalfunctionJun 24, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT THE SYRINGE 0.5ML 30GA 8MM 10BAG 500 PL/WG EXPERIENCED HUB SEPARATION FROM THE DEVICE DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO:928854 BATCH NO: 9161958. CONSUMER REPORTED ONE SYRINGE WOULD BE NUMBER 6 SYRINGE FROM BOX REMOVED SHIELD AND NEEDLE ASSEMBLE REMOVED WITH SHIELD ON (B)(6) 2020.

  Patient problems: No Patient Involvement

  MAUDE report 10187911 ↗
• MalfunctionMay 11, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED BEFORE USE THE SYRINGE 0.5ML 30GA 8MM 10BAG 500 PL/WG WAS FOUND WITH NO LABEL OR MISSING LABEL INFORMATION OR ILLEGIBLE (ALL PACKAGING LEVELS). THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PHARMACIST REPORTED THE EXPIRATION DATE WAS MISSING FROM THE BOX.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10045750 ↗
• MalfunctionJan 3, 2020Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT THERE WAS LIQUID FOREIGN MATTER INSIDE THE BARREL WITH A BD SYRINGE 0.5ML 30GA 8MM. THIS OCCURRED ON 7 OCCASIONS PRIOR TO USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT THE CUSTOMER NOTICED WHAT SHE DESCRIBED AS "WATER" INSIDE BARREL OF SYRINGES. STATED, IT WAS A FEW DROPS ON NEEDLE TIP WHEN SHE PUSHED ON PLUNGER ROD. THE SYRINGES WERE NOT USED FOR INJECTION.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9545748 ↗
• MalfunctionApr 3, 2019Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT BD¿ SYRINGE 0.5ML 30GA 8MM 10BAG 500 PL/WG HAD MOISTURE INSIDE OF THE SYRINGE. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 928854. BATCH NO. 7352875. IT WAS REPORTED THAT THERE WAS MOISTURE INSIDE OF THE SYRINGE. VERBATIM: (B)(6) PHARMACIST REPORTED ON BEHALF OF CONSUMER THAT THERE WAS MOISTURE INSIDE OF THE SYRINGE BEFORE INJECTION. CONSUMER DOES NOT RE-USE SYRINGE, OCCURRENCE DATE IS UNKNOWN. LOT # 7352875, PRODUCT # 928854, EXPIRATION DATE WAS NOT PROVIDED. PHARMACIST GAVE CONSUMER A REPLACEMENT BOX, SENDING MAIL KIT AND REPLACEMENT PRODUCT TO PHARMACY.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8480144 ↗
• MalfunctionJun 28, 2018Device Contamination with Chemical or Other Material

  IT WAS REPORTED THREE BD¿ INSULIN SYRINGE WITH NEEDLES WERE FOUND WITH CLEAR LIQUID AT THE TIP OF THE NEEDLE. THERE WAS NO REPORT OF EXPOSURE, SERIOUS INJURY OR MEDICAL INTERVENTION.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7647688 ↗
• MalfunctionMay 18, 2018Component Missing

  IT WAS REPORTED THAT BEFORE USE A BD¿ SYRINGE WAS FOUND WITH " THE RUBBER STOPPER WAS MISSING BEFORE INJECTION." THERE WAS NO REPORT OF EXPOSURE, INJURY OR MEDICAL INTERVENTION NEEDED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7526096 ↗