CVS Health 998842Recalls & reported problems

Woonsocket Prescription Center, Incorporated · 30 Piece Wound Care Kit LG: 8 - Gauze Pads 4 IN x 8 IN (10.1 cm x 20.3 cm); 8 - Non-stick Pads 3 IN x 8 IN (7.6 cm x 20.3 cm); 5 - Surgical Pads 5 IN x 9 IN (12.7 cm x 22.8 cm); 4 - Transparent Dressings 4 IN x 4.75 IN (10.1 cm x 12 cm); 3 - Rolled Gauze 6 IN x 2 YDS (15.2 cm x 1.8 m); 2 – Paper Tape 1 IN x 10 YD (2.5 cm x 9.1 m) · Class 1

All models of CVS Health (16)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports: 0
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

Jun 22, 2022Open, Classified
The product falls apart during handling after removal from its primary packaging.
Z-1517-2022 · Root cause: Process control · Recall details · FDA record ↗

Device details

UDI-DI	`00050428297056`
Brand	CVS Health
Model	998842
Company	Woonsocket Prescription Center, Incorporated
Product code	OHO · First Aid Kit Without Drug
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	May 7, 2020

Device type (GMDN): First aid kit, non-medicated, single-use

A convenient collection of equipment and materials intended to be used in an emergency for the rapid, initial treatment of an injury. This device is typically used by emergency medical services (EMS), institutions, schools, the home, motor vehicles, and other public settings. This device does not contain medicinal substances/pharmaceuticals. This is a single-use device.

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Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
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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