DRG International, Inc. recalls
Every recall we track for DRG International, Inc. — 7 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from DRG International, Inc. peaked in 2024 (3); 7 since 2017.
All FDA recall records for DRG International, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 3 | 0 | 3 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled DRG International, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All DRG International, Inc. recalls
7 shown- Lower riskMedical device
DRG International, Inc. recalls Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);
DRG International recalls Sperm Ab ELISA test kits with model EIA-1826 due to potential false negative results. Affected kits sold worldwide, including US, NJ, and multiple international countries. Contact for remedy.
DRG InternationalJul 2, 2026 - Lower riskMedical device
DRG International, Inc. recalls Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Model/Catalog Number: EIA-4568 Product Description: T4 Total
DRG International recalls T4 Total ELISA kits (model EIA-4568) due to incorrect expiration dates on box labels, which could lead to inaccurate test results. Affected kits were sold between 2025-01-01 and 2025-03-31.
DRG InternationalJun 4, 2025 - Lower riskMedical device
DRG International, Inc. recalls DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361
DRG International recalls Hybrid-XL insulin model HYE-5361 due to calibration failures causing delayed results. Affected units have specific UDI and lot numbers.
DRGOct 7, 2024 - Lower riskMedical device
DRG International, Inc. recalls 17-OH Progesterone ELISA 96 well kit- An enzyme immunoassay for the quantitative in vitro diagnostic measurement of
DRG recalls 17-OH Progesterone ELISA kits with mismatched control ranges that could delay test results and pose a remote health risk. Affected kits have specific model and lot numbers.
DRGSep 13, 2024 - Lower riskMedical device
DRG International, Inc. recalls Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for
DRG International recalls Salivary Testosterone ELISA model SLV-3013 due to invalid controls causing repeated tests and delayed patient results. Affected units have specific lot numbers.
DRG InternationalJul 5, 2024 - Lower riskMedical device
DRG International, Inc. recalls C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, heparin- or citrate plasma) and urine. Catalog
DRG International recalls C-Peptide ELISA test kits where low standard optical density may cause invalid runs and delayed patient results. Affected kits have specific catalog numbers and expiration dates.
DRG InternationalDec 21, 2021 - Lower riskMedical device
DRG International, Inc. recalls Total Thyroxine (T4) ELISA; REF EIA-1781
DRG International recalls two lots of Total Thyroxine ELISA tests that expired before their shelf life, potentially delaying thyroid diagnosis and using patient samples.
DRG InternationalOct 18, 2021
DRG International, Inc. recall questions
How many recalls has DRG International, Inc. had?
7 recalls from DRG International, Inc. are on record with U.S. safety agencies, from 2021–2026.
What is the most recent DRG International, Inc. recall?
DRG International, Inc. recalls Sperm Ab ELISA; Model/Catalog Number: EIA-1826; Product Description: Sperm Ab ELISA (96 well plate test);, dated Jul 2, 2026. Every DRG International, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled DRG International, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new DRG International, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.