Every recall we track for Apollo Care, LLC — 28 in all — plus the complaints and injury reports the public filed about them.
Apollo Care recalls SEMAGLUTIDE 5mg vials due to potential particulate matter that could cause injection site reactions. Affected vials have specific NDC and lot numbers.
Apollo Care recalls SEMAGLUTIDE 4.5mg vials due to potential particulate matter. This could cause injection site reactions. Check NDC 71170-812-03 with specific lots for affected products.
Apollo Care recalls SEMAGLUTIDE 9mg vials due to particulate matter that could cause injection site reactions. Affected vials have specific NDC and lot numbers. Consumers should contact Apollo Care for details.
Apollo Care recalls SEMAGLUTIDE 10mg vials due to particulate matter that could cause injection site reactions. Affected vials have NDC 71170-722-02 and lot AC-017274, expiring Dec 2026.
Apollo Care recalls 20mg SEMAGLUTIDE vials due to nylon/polyamide and silk/proteinaceous particulate matter that could cause injection site reactions. Affected vials have specific NDC and lot numbers.
Apollo Care recalls 0.9mg SEMAGLUTIDE vials due to nylon/polyamide and silk/proteinaceous particulate matter that could cause injection site reactions.
Apollo Care recalls SEMAGLUTIDE 6.75mg vials due to particulate matter that could cause injection site reactions. Affected vials have specific lot numbers and expiration dates.
Apollo Care recalls SEMAGLUTIDE 2.5mg vials due to nylon/polyamide and silk/proteinaceous particulate matter that could cause injection site reactions.
Apollo Care recalls SEMAGLUTIDE 2.25MG vials due to particulate matter risk. Affected lots expire 11/24/2026 or 12/31/2026. Stop using if you have these vials.
Apollo Care recalls SEMAGLUTIDE 12.5MG vials due to nylon/polyamide and proteinaceous particulate matter that could cause injection site reactions.
Apollo Care recalls SEMAGLUTIDE 7.5mg vials due to nylon/polyamide and silk/proteinaceous particulate matter that could cause injection site reactions.
Apollo Care recalls Fentanyl 500mcg injections due to lack of assurance of sterility. This could cause infections if used improperly. Contact the manufacturer for details.
Apollo Care recalls VANComycin 2.5g injection (NDC 71170-224-50) due to lack of sterility assurance. This may cause infections if used improperly. Contact Apollo Care for details.
Apollo Care recalls Fentanyl 50 mcg/mL syringes due to lack of assurance of sterility. This could lead to infections if used improperly. Affected units have specific NDC and lot numbers.
Apollo Care recalls VANComycin 1g added to 250mL 0.9% Sodium Chloride Injection due to lack of assurance of sterility. This could cause infections if used improperly.
Apollo Care recalls VANComycin 1.25g injection (NDC 71170-264-25) due to lack of sterility assurance. This medication may cause infections if used improperly.
Apollo Care recalls specific ketamine injections due to lack of sterility assurance. Products with NDC 71170-050-05 and certain lot numbers may be contaminated. Consumers should contact the manufacturer for details.