Facility

Biomedical Polymers, Inc.

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

Key facts

1recalls · worst Class III

—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)	1220502
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	16 Chocksett Road Sterling, MA, US 01564
Registration status	Active · expires 2026
Parent company	BIOMEDICAL POLYMERS, INC. dba BMP Medical (owner-operator 9012278)
Brand names	Mosie Baby Kit

Activity by year

Recalls (1)

Devices registered here (1)

At Home Intravaginal Insemination System
Product code QYZ (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.6110

Recalls & enforcement

Class IIITerminated2019-09-18
The metal cannula of the device either broke and the broken piece left in the blood specimen tube, or slid back into the plastic portion of the device instead of piercing the tube.

All facilities operated by BIOMEDICAL POLYMERS, INC. dba BMP Medical

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. “Biomedical Polymers, Inc. (FEI 1220502) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1220502-biomedical-polymers-inc/

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