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CVS Health

WOONSOCKET PRESCRIPTION CENTER, INCORPORATED · Model 159520 · UDI-DI 00050428516874

LRR
10
510(k) clearances
13
Adverse events
30
Recalls
146
Facilities

Description

Antibacterial Rapid-Seal Wound Kit, 26 pieces: 1 - Antibacterial Rapid-Seal Wound Gel 0.3 FL OZ (8mL), 5 - Gauze Pads 2 IN x 2 IN (50 mm x 50 mm), 4 - Antiseptic Wipes 4 3/4 IN x 3 IN (120 mm x 196 mm), 5 - Antibacterial Fabric Bandages 3/4 IN x 3 IN (19 mm x 76 mm), 5 - Antibacterial Fabric Bandages 2 IN x 4 IN (50 mm x 101 mm), 4 - Non-stick Pads 2 IN x 3 IN (50 mm x 76 mm); 1 – Paper Tape roll 1/2 IN x 5 YD (12.7 mm x 4.5 m), 1 Carrying Case

Recalls

DateFirmReason
2026-03-27North American Rescue LLC.Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-04-05Certified Safety Mfg IncFirst aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer.
2022-03-11Total Resources IntlULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-11Total Resources IntlULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-02ASO LLCKits contained recalled acetaminophen.
2020-06-05HF Acquisition Co. LLCA missing component (hand suction pump) in the emergency medical kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.