Walgreens 676986Recalls & reported problems

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00311917025292), received between May 3, 2019 and Apr 27, 2022 — 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.

• MalfunctionApr 27, 2022Missing Information; Missing Information

  IT WAS REPORTED 2 BD¿ INSULIN SYRINGES WERE MISSING THE EXPIRATION DATE ON THE PACKAGING. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CONSUMER REPORTED NOT SEEING THE EXP DATE ON THIS BOX AND BAGS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14219192 ↗
• MalfunctionJan 4, 2022Defective Component; Device Contamination with Chemical or Other Material; Defective Component; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT BD SYRINGE 1.0ML 30GA 8MM EXPERIENCED DIFFICULT PLUNGER ROD MOVEMENT, AND FOREIGN MATTER IN THE FLUID PATH. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED PLUNGER ROD DIFFICULT TO MOVE. CONSUMER REPORTED LIQUID COMING FROM THE SYRINGE AFTER DEPRESSING THE PLUNGER ROD.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13160216 ↗
• MalfunctionJul 13, 2021Failure to Deliver; Failure to Deliver

  IT WAS REPORTED THAT 5 SYRINGES 1.0ML 30GA 8MM 10BAG 500 PL/WG WERE UNABLE TO DELIVER INSULIN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER STATED, NEEDLE WOULD NOT DRAW INSULIN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12157979 ↗
• MalfunctionJan 28, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT A SYRINGE 1.0ML 30GA 8MM 10BAG 500 PL/WG HAD MISSING LABEL INFORMATION BEFORE 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 Consequences Or Impact To Patient

  MAUDE report 11248512 ↗
• MalfunctionSep 17, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 1.0ML 30GA 8MM 10BAG 500 PL/WG WAS MISSING THE EXPIRATION DATE. THIS WAS DISCOVERED BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO:928853 BATCH NO: 4230851. IT WAS REPORTED THAT THEY FOUND AN UNOPENED NOT USED BOX OF SYRINGES WITHOUT THE EXPIRATION DATE ON THE BOX.

  Patient problems: No Patient Involvement

  MAUDE report 10549999 ↗
• MalfunctionAug 12, 2020Leak/Splash; Leak/Splash

  IT WAS REPORTED DURING USE THE BD¿ INSULIN SYRINGE THE PLUNGER ROD WAS DIFFICULT TO MOVE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE CUSTOMER "REPORTED PLUNGER ROD DIFFICULT TO MOVE."

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10399119 ↗
• MalfunctionJul 8, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 1.0ML 30GA 8MM 10BAG 500 PL/WG WAS MISSING THE EXPIRATION DATE. THIS WAS DISCOVERED BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO: 928853 BATCH NO: 9210952. IT WAS REPORTED BOXES DID NOT HAVE EXP DATES ON THEM.

  Patient problems: No Patient Involvement

  MAUDE report 10248375 ↗
• MalfunctionJun 2, 2020Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT SYRINGE 1.0ML 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. 3928853 BATCH NO. 6193972, 6347727. IT WAS REPORTED THAT EXPIRATION DATE IS MISSING FROM BOX.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10109695 ↗
• MalfunctionNov 22, 2019Failure to Deliver; Failure to Deliver

  MATERIAL NO. 928853 BATCH NO. UNKNOWN. IT WAS REPORTED THAT DURING USE OF THE BD¿ 1ML, 30G X 8MM INSULIN SYRINGE 3 SYRINGES WOULD NOT DRAW INSULIN FULLY INTO SYRINGE AND WOULD GO BACK INTO VIAL. THIS OCCURRED ON 3 SEPARATE OCCASIONS BUT THE DATE/TIME AND OR PATIENT INFORMATION IS UNKNOWN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED, SHE COULD NOT DRAW HER MEDICATION WITH 3 SYRINGES. STATED, THE INSULIN WOULD START TO ENTER THE BARREL, BUT THEN, GO BACK INTO VIAL.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9363486 ↗
• MalfunctionNov 21, 2019Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED THAT THE EXPIRATION DATE WAS MISSING FROM THE BD¿ INSULIN SYRINGE BOX LABEL BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "PHARMACY CALLED AND STATED HE GOT A NEW BOX AND DO NOT SEE AN EXPIRATION DATE ON THE BOX."

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9355198 ↗
• MalfunctionOct 8, 2019Leak/Splash; Leak/Splash

  MATERIAL NO.: 928853, BATCH NO.: UNKNOWN. IT WAS REPORTED THAT DURING USE OF THE BD¿ 1ML, 30G X 8MM INSULIN SYRINGE THE CONSUMER HAD DIFFICULTY IN MOVING THE PLUNGER DURING INJECTION AND WHEN DRAWING INSULIN. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: PLUNGER DIFFICULT TO MOVE DURING INJECTION AND WHEN HE'S DRAWING INSULIN. HE WAS STILL ABLE TO USE THE SYRINGES AND GET HIS COMPLETE DOSAGE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9166567 ↗
• MalfunctionAug 7, 2019Failure to Deliver; Failure to Deliver

  IT WAS REPORTED THAT AN UNSPECIFIED NUMBER OF SYRINGE 1.0ML 30GA 8MM 10BAG 500 PL/WG EXPERIENCED AN INABILITY OR DIFFICULT ASPIRATING DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO. 928853 BATCH NO. 8176693. VERBATIM: CONSUMER REPORTED THAT HIS SYRINGE WILL NOT DRAW THE INSULIN, STATED THAT HE IS NEW TO USING SYRINGES, DOES NOT RE-USE. LOT # 8176693, PRODUCT # 928853, NO EXP DATE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8872025 ↗
• MalfunctionMay 3, 2019Leak/Splash; Leak/Splash

  IT WAS REPORTED THAT PLUNGER WAS DIFFICULT TO MOVE AND LEAKAGE OCCURS BECAUSE WHEN PULLED TOO HARD PLUNGER COMES OUT AND MEDICATION LEAKS WITH BD¿ 1ML, 30G X 8MM INSULIN SYRINGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED IT TAKES HER A FEW TRIES WITH DRAWING HER 85 UNITS BECAUSE IT'S HARD TO PULL ON PLUNGER ROD. STATED THERE ARE TIMES WHEN SHE HAS PULLED THE PLUNGER ROD COMPLETELY OUT AND WASTED MEDICATION. STATED THE SYRINGE IS A POOR DESIGN AND PLUNGER ROD SHOULD HAVE SOMETHING ON THE END TO PREVENT IT FROM COMING OUT. STATED THE NEEDLE IS NOT SHARP/DULL. NO INJURY

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8579156 ↗