Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks
Arrow International Inc. is recalling 9 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device with a defect that may result in reduced drug delivery and inadequate pain relief, representing a risk of harm where injury has not yet been reported.
Plain-English summary
Arrow International Inc. is recalling 9 units of the Arrow AutoFuser Disposable Pain Control Pump (Product code MC0050XL CPNB). The recall is due to possible cracks on the body of the fill port connector, which may result in a leak.
If a leak is identified while the user is filling the pump, there may be a delay while an alternative pump is located. If the leak goes undetected, it may result in a reduced level of drug delivery to the patient and consequently a lower level of pain relief than prescribed or expected. This may result in the need for other, additional analgesic drug administration.
The affected units were distributed nationwide. Consumers and healthcare providers should check their inventory for the specific lot codes listed in the recall notice and contact the manufacturer for further instructions.
The recalled product
- Product
- AF 550 x 5ML/HR CPNB, Product code MC0050XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Pain Management
- Affected units
- 9
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 17 recalled by Arrow International 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.
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