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Company name: Purina Animal Nutrition
Brand name: Purina
Product recalled: Supplement feed for cattle livestock and for wildlife such as deer, antelope, and wild sheep
Reason of the recall: potential of elevated urea levels
FDA Recall date: October 27, 2021
Recall details: Company Announcement Purina Animal Nutrition... See More is voluntarily recalling one lot of the following products for cattle livestock and for wildlife such as deer, antelope, and wild sheep due to the potential of elevated urea levels. The affected products include:
Check the full recall details on fda.gov
Source: FDA
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Company name: Windstone Medical Packaging dba Aligned Medical Solutions
Brand name: Cardinal Health’s Monoject™
Product recalled: Flush Prefilled Saline Syringes
Reason of the recall: Potential for the plunger to draw back after the air has been expelled and reintroduced air back into the syringe
FDA Recall date:... See More October 27, 2021
Recall details: Company Announcement On August 19, 2021, Aligned Medical Solutions initiated a nationwide recall of Cardinal Health’s Monoject™ Flush Prefilled Saline Syringes placed into 9,378 kits. Including; 1 lot of AMS-9041CP Leaderflex Insertion Kit with Ultrasound
1 lot of AMS-9046CP-1 Insertion Tray-RX
45 lots of AMS8939A Universal Procedure Pack w/Split Drape
1 lot of AMS9957A Port Insertion Pack
3 lots of AMS12149 Procedure Pack
These convenience kits have been found to contain the Cardinal Health’s Monoject™ Flush Prefilled Saline Syringe part # 8881570121, which has been recalled for the potential for the plunger to draw back after the air has been expelled and reintroduced air back into the syringe. If a clinician is not aware of air being introduced into the syringe, the clinician could inadvertently push air into the vascular system creating the potential for an air embolism. Injection of air into the vascular system can cause air embolism which can result in serious adverse health consequences or death. See Cardinal Health’s Urgent Medical Device Recall Event 2021-04063 Monoject™ Flush Prefilled Saline Syringes cardinalhealth.com Consumers who have affected product(s) should immediately review their inventory and quarantine all affected kits. Contact the Quality Department for further instructions on labeling and replacement product if needed at 407-638-9924. Customers will be provided with a yellow label that is to be placed on the packs containing the recalled Cardinal Health’s Monoject™ Flush Prefilled Saline Syringe. The label will read as follows; At the time the kit is opened for use the prefilled syringe manufactured by Cardinal Health should be identified, set aside and not used. Do not use the prefilled syringe in the kit.
The recalled prefilled syringe should be rendered unusable to protect against inadvertent use and disposed or pursuant to the medical waste policies in effect at your institution
Consumers can request replacement syringes by calling 407-638-9924. Recalled Product(s) were manufactured from 01/13/2020 to 10/14/2020 and distributed from 01/23/2020 to 10/19/2020. The following kit part numbers and lot numbers containing the recalled /affected Cardinal Health Monoject™ Flush Prefilled Syringes have been recalled:
Check the full recall details on fda.gov
Source: FDA
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