Showing 61–80 of 422 alerts
FDA Food Recall Announcement - Pending Structured Confirmation
2026 record
Source: FDA-ANNOUNCE
Aquafaba Powder 4oz (113g) and (12 oz (340g) flexible foil pouches Announced by FDA
July 30, 2026
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FDA Food Recall Announcement - Pending Structured Confirmation
2026 record
Source: FDA-ANNOUNCE
Organic IQF Frozen Blueberries and Whole Mixed Berries, 10 oz and 48 oz Announced by FDA
July 30, 2026
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Drug Recall
2026 record
Source: FDA
CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc., Tarrytown, NY 10591, a Prestige Consumer Healthcare Company. NDC: 67172-999-01 UPC 6 78112 65920 3 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04. Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (5mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202.NDC 71170-712-03 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Drug Recall
2026 record
Source: FDA
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05 Recall initiated
July 29, 2026 Reported by FDA
August 19, 2026
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Food Recall
2026 record
Source: FDA
Kerry, Inc Recall initiated
July 29, 2026 Reported by FDA
August 12, 2026
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Food Recall
2026 record
Source: FDA
FlavorsandColor.Com Recall initiated
July 28, 2026 Reported by FDA
August 19, 2026
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FDA Food Recall Announcement - Pending Structured Confirmation
2026 record
Source: FDA-ANNOUNCE
Eridanous Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling, 11.6 oz (330 g), UPC 4056489125839 Announced by FDA
July 28, 2026
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FDA Announcement - Pending Structured Confirmation
2026 record
Source: FDA-ANNOUNCE
Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL Announced by FDA
July 27, 2026
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Food Recall
2026 record
Source: FDA
Big Way Ca Inc Recall initiated
July 24, 2026 Reported by FDA
August 12, 2026
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FDA Announcement - Pending Structured Confirmation
2026 record
Source: FDA-ANNOUNCE
Cefazolin in Dextrose Injection Announced by FDA
July 24, 2026
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Data last updated: September 5, 2026 ET
Investigations and recalls may be ongoing; status, case counts, and guidance are updated by the source agency as events continue.
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