Facility

APOTHECARY PRODUCTS, LLC.

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

Key facts

1recalls · worst Class II

2inspections · worst VAI

—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)	2183416
Establishment type	Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Repack or Relabel Medical Device
Location	11750 12th Ave S BURNSVILLE, MN, US 55337
Registration status	Active · expires 2026
Parent company	APOTHECARY PRODUCTS, LLC (owner-operator 2183416)
Brand names	Flents Finger Sleeve: F414-417

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Dressing, Compression
Product code MHW (opens in a new tab) · Class I · General Hospital · 21 CFR 880.5075

Recalls & enforcement

Class IIOngoing2023-03-30
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.

FDA inspections (2)

NAI2019-09-03
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
NAI2016-05-05
No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

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. “APOTHECARY PRODUCTS, LLC. (FEI 2183416) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2183416-apothecary-products-llc/

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