AlereTM

Alere™ hCG Combo Cassette (25mIU/mL) in Urine (CLIA Waived) or Serum

Registry build 21.09.26
16manufacturers in China registered for this device type
5catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Zhejiang (5), Guangdong (3), Beijing (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JHI
Manufacturer City Province Registered as Device types
Hangzhou Biotest Biotech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 41
Abon Biopharm (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 17
Planet(Shanghai) International Co., Ltd. Shanghai Shanghai Exporter 93
Hangzhou AllTest Biotech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 48
Assure Tech. (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 48
Guangzhou Wondfo Biotech Co., Ltd. Guangzhou Guangdong Contract manufacturer 44
W.h.p.m. Bioresearch & Technology Co., Ltd. Beijing Beijing Manufacturer 37
Beijing Choice Electronic Technololgy Co., Ltd. Beijing Beijing Repacker / relabeller 30
Taizhou Chenguang Import AND Export Trading Co., Ltd. Taizhou Jiangsu Exporter 25
Chong Qing Teco Huayi Pharm. Co. Shapingba Dist. Chongqing Contract manufacturer 18
Anhui Deepblue Medical Technology Co., Ltd. Hefei Anhui Contract manufacturer 16
Hangzhou Aichek Medical Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 13

Showing 12 of 16. All 16 manufacturers in China registered for Visual, Pregnancy Hcg, Prescription Use

Record

Regulatory record for AlereTM
Listed by Alere San Diego, Inc., United States
FDA product code JHI
Device type Visual, Pregnancy Hcg, Prescription Use
Device class Class 2
Regulation 21 CFR 862.1155
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
Record revised 2026-03-13 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for AlereTM
Catalogue number Size Per pack Status
92211 50 In distribution
92225 40 In distribution
92215 40 In distribution
92210 30 In distribution
92217 40 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
McKesson Mckesson Medical-Surgical Inc. 7
Cardinal Health Cardinal Health 200, LLC 7
Rapid Response Btnx Inc. 7
Visual, Pregnancy Hcg, Prescription Use W.h.p.m., Inc. 6
Preview Wondfo USA Co., Ltd. 6
Sure-Vue Fisher Scientific Company L.L.C. 6
Wondfo Wondfo USA Co., Ltd. 6
Aimstep Pregnancy Germaine Laboratories, Inc. 5
Detector hCG Immunostics, Inc. 5
QuickVue Quidel Corp. 5
Medline Medline Industries, Inc. 5
Henry Schein Henry Schein, Inc. 4

Showing 12 of 113. All products under Visual, Pregnancy Hcg, Prescription Use

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of AlereTM
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Mckesson Medical-Surgical Inc. Corporate Office UDI-DI 2022-05-25 Class II Environmental control Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. a. 5 kits b. 12 kits

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Class III is unlikely to cause harm at all → typically a labelling or documentation fault. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-04-16 Class II Packaging The firm initiated recall of Alere” hCG Combo Cassette (20/10 mIU/mL) kit PN 92215, lots hCG1110133 and hCG1110135, because an investigation has indicated a portion of these Alere” hCG Combo Cassette (20/10 mIU/mL) PN 92215 kit lots were in 3975 kits 2013-10-18
2013-01-21 Class III Labeling mix-ups Alere San Diego Inc. is recalling the Cardinal Health hCG Cassette Rapid Test because some of them were incorrectly packaged into Cardinal Health hCG Combo Rapid test kit boxes. The kit box incorrectly indicates the product may be used for 2,167 kits 2013-08-28

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer