WalgreensRecalls & reported problems across all models
Walgreen CO. · 38 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 395
- Deaths reported
- 0
- Injuries reported
- 26
- Recalls
- 0
We found 38 models of Walgreens by Walgreen CO. in the FDA's device registry (GUDID). Together they are named in 395 adverse event reports in the FDA's MAUDE database, received between Nov 11, 2015 and Sep 30, 2026 — classified as 26 injuries, 369 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (83 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
Reports received per month, all models
Most reported Walgreens problems
Device problems
- No Apparent Adverse Event99
- Leak/Splash83
- False Positive Result51
- False Negative Result43
- Device Markings/Labelling Problem35
- Failure to Deliver33
- Break28
- Device Contamination with Chemical or Other Material28
Patient problems
- No Clinical Signs, Symptoms or Conditions208
- No Known Impact Or Consequence To Patient85
- No Consequences Or Impact To Patient44
- No Patient Involvement19
- Insufficient Information6
- Pain5
- Fall4
- No Information4
Walgreens models
38 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Walgreens 505288Coronavirus Antigen Detection Test System.99 reports
- Walgreens 654882Syringe, piston62 reports
- Walgreens 654878Syringe, piston49 reports
- Walgreens 654567Syringe, piston39 reports
- Walgreens 677257Syringe, piston22 reports
- Walgreens 490530Aid, Transfer22 reports
- Walgreens 677259Syringe, piston18 reports
- Walgreens 676988Syringe, piston14 reports
- Walgreens 676987Syringe, piston13 reports
- Walgreens 676986Syringe, piston13 reports
- Walgreens 677258Syringe, piston5 reports
- Walgreens 218257Vinyl Patient Examination Glove5 reports
- Walgreens 2100-WGNHumidifier, Non-Direct Patient Interface (Home-Use)2 reports
- Walgreens 400195Wheelchair, Mechanical2 reports
- Walgreens 276733Adaptor, Hygiene2 reports
- Walgreens 276741Walker, Mechanical2 reports
- Walgreens 931979Tape And Bandage, Adhesive2 reports
- Walgreens 940856Dressing, Wound, Drug2 reports
- Walgreens 940859Dressing, Wound, Drug2 reports
- Walgreens 381506Walker, Mechanical2 reports
- Walgreens 319600Polymer Patient Examination Glove1 report
- Walgreens 407160Polymer Patient Examination Glove1 report
- Walgreens 350716Vinyl Patient Examination Glove1 report
- Walgreens 830427Tape And Bandage, Adhesive1 report
- Walgreens 831245Tape And Bandage, Adhesive1 report
- Walgreens 426041Vinyl Patient Examination Glove1 report
- Walgreens 153122Gauze / Sponge,Nonresorbable For External Use1 report
- Walgreens 153123Gauze / Sponge,Nonresorbable For External Use1 report
- Walgreens 156744Strip, Adhesive, Closure, Skin1 report
- Walgreens 276735Adaptor, Hygiene1 report
- Walgreens 344345Dressing, Wound, Occlusive1 report
- Walgreens 369353Adaptor, Hygiene1 report
- Walgreens 369359Adaptor, Hygiene1 report
- Walgreens 940858Dressing, Wound, Drug1 report
- Walgreens 990443Dressing, Wound, Occlusive1 report
- Walgreens 785410Tape And Bandage, Adhesive1 report
- Walgreens 400577Dressing, Wound, Occlusive1 report
- Walgreens 109881Tape And Bandage, Adhesive1 report
Recent Walgreens adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Activation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952432 ↗MalfunctionSep 30, 2026Damaged Thread
It was reported that the threaded insert for one of the rear legs is stripped, customer states the knob will not stay tightened down because of this. Customer swapped various knobs and none of them tighten.
Patient problems: Fall
MAUDE report 50947016 ↗MalfunctionSep 30, 2026Unstable
It was reported that "when to unlock it from locked and it flopped" and "Rollator hand brake lever is just floppy not staying firm in its place."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944869 ↗MalfunctionSep 29, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937110 ↗MalfunctionSep 26, 2026Volume Accuracy Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907925 ↗MalfunctionSep 26, 2026Volume Accuracy Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907905 ↗MalfunctionSep 26, 2026Volume Accuracy Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907891 ↗MalfunctionSep 26, 2026Volume Accuracy Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907876 ↗MalfunctionSep 26, 2026Volume Accuracy Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907828 ↗MalfunctionSep 26, 2026Vibration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907798 ↗MalfunctionSep 26, 2026Volume Accuracy Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50907748 ↗MalfunctionSep 25, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50904065 ↗MalfunctionSep 25, 2026Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50899295 ↗MalfunctionSep 25, 2026Delivered as Unsterile Product
Pharmacist Reported was dispensing a 10 packet to patient and noticed 3 syringes in sealed bag without needle shields. Discard Lot # 2206101Catalog# Walgreens syringe 928850 Date of Event 06.17.2024Sample Status 06.17.2024------------------------------------------------------------This intake record was reviewed as part of CAPAs #PR-00078 and #PR-00080 and deficiencies were identified. The following actions were taken, Two additional complaint record was created for Shield Missing. With these actions completed, this Intake record is now consistent with applicable procedures CP62096, CP92021, and regulatory requirements, and separate complaints were opened for each separate event. There was appropriate follow-up (if this was required), and each event is addressed based on the most current information. No further action is required at this time unless new information becomes available. R. Rozenberg 14SEP2026
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898815 ↗MalfunctionSep 25, 2026Delivered as Unsterile Product
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50898191 ↗
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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