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Bloodborne Pathogen Cabinet Refill - 100 Piece
ULINE, INC. · Model S-21103 · UDI-DI 10851253007684
10
510(k) clearances
13
Adverse events
30
Recalls
143
Facilities
Description
"(4) ABSORBENT POWDER (41) ANTISEPTIC TOWELETTE (4) BAG WITH SCOOP (4) BIOHAZARD BAG (4) BOUFFANT CAP (1) GERMICIDAL SPRAY (4) GOWN (31) HAND SANITIZER (14) NITRILE GLOVES (18) PAPER TOWEL (4) DISPOSABLE FACE MASK WITH SHIELD (4) SHOE COVERS (7) GERMICIDAL WIPES"
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-27 | North 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 |
| 2022-06-23 | Family Dollar Stores, Llc. | Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022. |
| 2022-04-05 | Certified Safety Mfg Inc | First aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer. |
| 2022-03-11 | Total Resources Intl | ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due |
| 2022-03-11 | Total Resources Intl | ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due |
| 2022-03-02 | ASO LLC | Kits contained recalled acetaminophen. |
| 2020-06-05 | HF Acquisition Co. LLC | A missing component (hand suction pump) in the emergency medical kits. |
| 2020-06-04 | HF Acquisition Co., LLC | Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. |
| 2020-06-04 | HF Acquisition Co., LLC | Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. |
| 2020-06-04 | HF Acquisition Co., LLC | Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. |
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Get your free API keyRead the docsData 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.