Twenty-First Century Healthcare, Inc Recall: 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co Q10 200mg 30ct capsules due the product being mislabeled and potentially containing Vit D 2000 IU.

🇺🇸 United States

1. January 22, 2019 - Recall initiated
2. March 13, 2019 - Reported by source
3. August 29, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1147-2019

Event ID

82282

Status

Terminated

Classification

Class III

Company

Twenty-First Century Healthcare, Inc

Product description

Good Neighbor Pharmacy, D 2000 IU, Dietary Supplement, UPC: 0-87701-40751-2, 30 tablets.

Quantity

5,484 bottles (total)

Reason

21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co Q10 200mg 30ct capsules due the product being mislabeled and potentially containing Vit D 2000 IU.

Recall initiation date

January 22, 2019

Report date

March 13, 2019

Classification date

Not published in this source record

Termination date

August 29, 2019

Distribution pattern

Nationwide. 14 DCs and distributor. No foreign/VA/govt/military consignees.

UPC, lot, and code information

UPC 0-87701-40751-2; Lot Number: 12921101 Exp Date: 06/21 Product Number: 0-87701-40751-2

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 82282 with 1 other product entry in Public Health Trace.

Responsible company: Twenty-First Century Healthcare, Inc

Other recalls from Twenty-First Century Healthcare, Inc

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Virginia	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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