Bion Enterprises IgG FITC Conjugate Recalled for Incorrect Expiration Date
Bion Enterprises is recalling 504 units of IgG FITC Conjugate because the labeled expiration date is one year too long.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which by definition is unlikely to cause adverse health consequences. The issue is a minor labeling error regarding the expiration date.
Plain-English summary
Bion Enterprises Ltd is recalling 504 units of IgG FITC Conjugate, a plastic bottle containing 3.5 mL of product used as a counterstain for various indirect fluorescent assay kits. The recall is due to a labeling error where the affected products have a labeled expiration date that is one year too long.
The affected products are identified by Product Code CCG-9972 and Lot CCG-0281. These units were distributed worldwide, including in the United States (specifically in Indiana and South Carolina), Canada (Toronto), South Africa (Randburg), and Brazil (Rio de Janeiro).
Consumers and laboratories should stop using the affected product and contact the manufacturer for further instructions.
The recalled product
- Product
- Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Usage: Product is a used as a counterstain for various indirect fluorescent assay kits
- Manufacturer
- Bion Enterprises Ltd
- Hazard
- Affected units
- 504
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Product Code: CCG-9972
- Lot: CCG-0281
Distribution
Part of a larger recall action
This product is one of 3 recalled by Bion Enterprises Ltd under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
Same manufacturer · Bion Enterprises Ltd
See all →- LowBion Enterprises IgM Conjugate Recalled for Incorrect Expiration Date Labeling
FDA (Devices) · 2013-06-12
- LowBion Enterprises IgG Conjugate Recalled for Incorrect Expiration Date Labeling
FDA (Devices) · 2013-06-12
Same hazard · mis labeling
See all →- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- HighByron White A-L Complex Herbal Supplement Recalled for Undeclared Walnut
FDA (Food) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02