# FDA recall Z-1060-2022

> **Certified Safety Mfg Inc** · Class II · device recall initiated 2022-04-05.

## Product

The following first aid kits and cabinets containing components Medi-First XS Non-Aspirin, Product #80450, 2 tablets/packet, 25 packets/box; and Sinus Pain & Pressure, Product #81950, 2 tablets/packet, 25 packets/box.     Product number and description:    (1) K614-020 16PW - Firestone Supplemental - w/Logo;  (2) KR614-020 16R - Firestone Supplemental - Refill;  (3) K616-033 36M - Class A Office - Metal;  (4) KR616-006 36R - Class A Office - Refill;  (5) KR616-015 75R - Class A Office - Refill;  (6) K616-015 75V - Class A Office - 3-Shelf Cabinet;  (7) K618-016 EMT - Duke Energy TD - Red Bag;  (8) KR618-016 EMTR - Duke Energy TD - Refill;  (9) K616-008 FAC-3 - Class B + Meds - 3 Shelf Cabinet;  (10) KR616-008 FAC-3R - Class B + Meds - Refill;  (11) K618-013 FAC-3 - Five Star Safety - w/Logo;  (12) K611-044 FAC-3 - Uline 100 person - w/Logo;  (13) K620-609 FAC-3 - Uline Class B + Meds - w/Logo;  (14) K616-072 FAC-4 - Choate Construction - w/Logo;  (15) KR616-072 FAC-4R - Choate Construc

## Reason for recall

First aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer.

## Distribution

Distribution was made to AL, AZ, CA, CO, CT, FL, GA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TX, UT, VA, WA, WI, WV, and WY.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-1060-2022
- **Recalling firm:** Certified Safety Mfg Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-05
- **Report date:** 2022-05-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kansas City, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1060-2022

## Citation

> AI Analytics. FDA recall Z-1060-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1060-2022. Source: US FDA. Licensed CC0.

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