Molded Products Recalls Mislabelled Luer Lock Sets for IV Administration
Molded Products Inc is recalling 130,000 Luer Lock Sets (Catalog # MPC-125) because some packages were incorrectly labeled as a different product.
What this means for you
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 involves a minor labeling error where packages were misidentified as a different catalog number, without reported injuries or illnesses.
Plain-English summary
Molded Products Inc is recalling 130,000 Luer Lock Sets, Catalog # MPC-125, intended for IV administration sets. The recall was initiated because some unit of sale packages, specifically bags of 100 sets, were found to be incorrectly labeled as Molded Products Male to Male Luer Adapters, Catalog # MPC-150.
The affected products are distributed nationwide in the United States. The specific lot number is 20266, with a UDI of +B144MPC1251/$$52232420266N and an expiration date of 11/20/2022.
Healthcare providers and consumers should check their inventory for these specific packages. If the product matches the description and lot number, it should be removed from use and returned to the distributor or manufacturer according to their instructions.
The recalled product
- Product
- Luer Lock Set - Catalog # MPC-125, for IV administration sets.
- Manufacturer
- Molded Products Inc
- Hazard
- Affected units
- 130,000
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- LOT NUMBER: 20266 UDI # +B144MPC1251/$$52232420266N Expiration Date 11/20/2022
Distribution
Distributed nationwide across the United States.
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