Hartley Medical Center Pharmacy Recalls Morphine Sulfate Syringes for Sterility Concerns
Hartley Medical Center Pharmacy is recalling two syringes of Morphine Sulfate 0.6 mg/ml due to a lack of assurance of sterility.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, which corresponds to a Severe severity score under the rubric for significant injury or property damage reports or high-risk scenarios.
Plain-English summary
Hartley Medical Center Pharmacy, Incorporated is recalling two syringes of Morphine Sulfate 0.6 mg/ml, 200 ml volume, prescription only. The recall was initiated because of a lack of assurance of sterility for the product.
The affected product has a beyond-use date of May 3, 2016. The recall is limited to the United States, with no foreign distribution reported.
Consumers and healthcare providers should stop using the affected syringes and contact the recalling firm for further instructions or a replacement.
The recalled product
- Product
- Morphine Sulfate 0.6 mg/ml, vol. 200 ml syringe, Rx only, Hartley Med Ctr Pharmacy, Long Beach, CA
- Manufacturer
- Hartley Medical Center Pharmacy, Incorporated
- Category
- Drug — Injectable Medication
- Hazard
- Affected units
- 2
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)
- BUD: 5/3/2016
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 30 recalled by Hartley Medical Center Pharmacy, Incorporated under a single FDA (Drugs) 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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