Cadence Recalls Perfectum Tuberculin Glass Syringes Due to Misaligned Marks
Cadence Inc. is recalling 766 non-sterile Perfectum Tuberculin Glass Syringes because graduation marks are not centered with numeric position marks.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the defect involves a labeling/measurement alignment issue without reported injuries, fitting the criteria for moderate severity.
Plain-English summary
Cadence Inc. is recalling 766 units of Perfectum Tuberculin Glass Syringes, Non sterile, catalog numbers 5202, 5205, and 5212. The recall is due to a defect where the graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.
The affected products were distributed nationwide and to foreign locations including Canada, Denmark, and Italy. Specific packaged lots are identified in the recall documentation for each catalog number.
Consumers and healthcare providers should stop using the affected syringes and contact Cadence Inc. for instructions on return or replacement.
The recalled product
- Product
- Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
- Manufacturer
- Cadence Inc.
- Category
- Medical Device — Syringes
- Hazard
- Affected units
- 766
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 (17)
- Packged Lots: Catalog Number 5202: 79713-04
- 80468-05
- W003542/1
- W006324/1
- W006324/2
- W006324/3
- W006324/4
- W006324/5
- Catalog Number 5205: 79748-03
- Catalog Number 5212: W008136/1
- W008686/1
- W011240/1
- W010905/1
- W012135/1
- W014053/1
- W015838/1
- W011240
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Cadence Inc. 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 2 products in this recall →Related recalls
Same manufacturer · Cadence Inc.
See all →- ModerateCadence Micro-Mate Tuberculin Glass Syringes Recalled for Misaligned Graduation Marks
FDA (Devices) · 2015-08-19
Same hazard · mis labeling
See all →- High
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