Dried Blood Control

MassCheck® Amino Acids, Acylcarnitines EXTENDED incl. Ado, dAdo Dried Blood Spot Control Level III

Registry build 21.09.26
1manufacturer
8catalogue numbers in this listing
7recalls on this code

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code JJY
Manufacturer City Province Registered as Device types
Getein Biotech, Inc. Nanjing Jiangsu Manufacturer 19

Record

Regulatory record for Dried Blood Control
Listed by Chromsystems Instruments & Chemicals Gmbh, Germany
FDA product code JJY
Device type Multi-Analyte Controls, All Kinds (Assayed)
Device class Class 1
Regulation 21 CFR 862.1660
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2025-07-31

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, expiry date
Storage Storage environment temperature up to -18 °C

Catalogue Numbers

Catalogue numbers for Dried Blood Control
Catalogue number Size Status
0197 1 x 3spots In distribution
0192 1 x 3spots In distribution
0196 1 x 3spots In distribution
0296 1 x 3spots In distribution
0193 1 x 3spots In distribution
0195 1 x 3spots In distribution
0297 1 x 3spots In distribution
0295 1 x 3spots In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Liquichek Bio-Rad Laboratories Inc. 154
Validate LGC Clinical Diagnostics, Inc. 120
InteliQ Bio-Rad Laboratories Inc. 50
Lyphochek Bio-Rad Laboratories Inc. 39
Stat Profile Nova Biomedical Corporation 38
i-STAT Abbott Point OF Care Inc. 24
Multichem AE Techno-Path Manufacturing Ltd. 20
Serum Control Chromsystems Instruments & Chemicals Gmbh 18
BioPlex 2200 Bio-Rad Laboratories Inc. 16
Nova Nova Biomedical Corporation 14
Plasma Control Chromsystems Instruments & Chemicals Gmbh 14
Multichem IA Speciality Techno-Path Manufacturing Ltd. 12

Showing 12 of 559. All products under Multi-Analyte Controls, All Kinds (Assayed)

Recalls Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Dried Blood Control
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Chromsystems Instruments & Chemicals Gmbh UDI-DI 2022-05-19 Class II Labeling Change Control Too low concentration of glycine was detected in the dried blood controls of the batch 2821 of the products. 1330 units 2024-05-15
Chromsystems Instruments & Chemicals Gmbh UDI-DI 2022-05-19 Class II Labeling Change Control Too low concentration of glycine was detected in the dried blood controls of the batch 2821 of the products. 1457 units 2024-05-15

Recalls

5 of these are Class II. Class II means a temporary or reversible health consequence. 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
2020-11-02 Class II Under Investigation by firm XXX 342 vials 2021-12-20
2020-11-02 Class II Under Investigation by firm XXX 363 vials 2021-12-20
2020-11-02 Class II Under Investigation by firm Products do not meet stability criteria and may impact results. 362 vials 2021-12-20
2020-10-29 Class II Under Investigation by firm Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone. 880 vials
2020-10-29 Class II Under Investigation by firm Control lots may not meet stability criteria and could result in increased results of patient samples for cortisone. 850 vials

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