Facility

ECOLAB FOOD SAFETY SPECIALTIES INC.

8 recall(s) on record — most severe on record: Class II.

Key facts

8recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3013545043
Establishment type	Manufacture Medical Device
Location	2152 RIVERBEND Drive West Fort Worth, TX, US 76118
Registration status	Active · expires 2026
Parent company	Ecolab Inc (owner-operator 9009921)
Brand names	ECOLAB Carepod First Aid Kit; ECOLAB Essentials First Aid Kit

Activity by year

Recalls (8)

Devices registered here (1)

First Aid Kit With Drug
Product code LRR (opens in a new tab) · Not classified · Unknown

Recalls & enforcement

Class IITerminated2021-01-11
Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc Drapes from a single lot. A source for potential manufacturing error was identified and investigation is underway to prevent further recurrence. The slits may lead to a breach in the sterile barrier between fl…
Class IITerminated2018-09-14
The pouches of certain lots of product may have wrinkles along the pouch seal that could result in a channel within the seal. Should there be a channel in the pouch seal it may result in a breach in the sterility of the product.
Class IIITerminated2017-11-22
The incorrect IFU was shipped with the product.
Class IITerminated2017-10-13
Sterile packaging of the disposable light handle cover may contain gaps in the seal of the pouch.
Class IIITerminated2016-11-30
The reason for the recall is that the inner carton box of the Rolled Probe Cover PC0907NB has the incorrect expiration date (2015-10-01) on the label while the individual pouch labels and outer shipper have the correct expiration date (2018-10-01). The manufacturing date was ina…
Class IITerminated2016-07-14
Ecolab is recalling 2 models of Angiography Drapes with Radiation Shields because the sterile packaging may contain small holes in the film of the pouch.
Class IITerminated2015-08-18
The sterile packaging may contain small (less than 250 microns wide) channels in the seal of the pouch. If channels are present, the package integrity is compromised and there is a remote chance that a non-sterile drape may be used during a surgical procedure.
Class IITerminated2013-07-02
Certain lots of these Bur Hole Probe Covers did not undergo endotoxin (LAL) testing to the proper levels.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “ECOLAB FOOD SAFETY SPECIALTIES INC. (FEI 3013545043) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3013545043-ecolab-food-safety-specialties-inc/

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