Recall archive
31,892 recalls · page 121 of 1329
Reported Sep 10, 2025
MI Cancer Seek REF MSC000 UDI Code: (01)00860008613325(21)H5HJHDSXF MI Cancer Seek is a single-site assay intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caris Life Sciences
FDA (openFDA device enforcement)
Reported Sep 10, 2025
CHETAK LLC GROUP recalls Deep Frozen fruits and vegetables due to Salmonella
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Chetak LLC Group
FDA (recalls & safety alerts)
Reported Sep 10, 2025
DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.DermaRite Industries, LLC
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 10, 2025
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM Android App Model/Catalog…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dexcom, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Product Name: Blueberry Pretzels " Brand Name: HEB " Description: 8oz HEB Blueberry Flavored Yogurt Pretzels " UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollins Pecan Co., Inc.
FDA (openFDA food enforcement)
Reported Sep 10, 2025
Evergreen Farm Korean Pear Juice, 4 fl. oz. (120ml) , Foil pouches, 25 foil pouches per case, Refrigerate product after…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Evergreen Orchard Farm, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 10, 2025
FloPatch FP120, REF: FP120-FOT01-005
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Flosonics Medical (R/A 1929803 ONTARIO CORP.)
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Gina Marie Bakery recalls No Brand Cookies due to Undeclared almonds, sesame, Red 40, Red 3, Blue 1, Yellow 5, Red 40, Yellow 6
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Gina Marie Bakery
FDA (recalls & safety alerts)
Reported Sep 10, 2025
Hans Kissle Red Bliss Potato Salad
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hans Kissle Company, LLC
FDA (openFDA food enforcement)
Reported Sep 10, 2025
Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included. 50mL, Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Immunocore, LLC
FDA (openFDA drug enforcement)
Reported Sep 10, 2025
Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Lemon Meringue Pie, 8" round. Net Wt. 27 OZ; Refrigerate after opening Item Code 31811; UPC: 8 85523 31811 1;Jessie's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jessie Lord Bakery, LLC
FDA (openFDA food enforcement)
Reported Sep 10, 2025
Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product Name: 900-00218 Sterile Cover 10-Pack Shipper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumicell, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Medshape Universal Joints, REF: DNE-9000-UJ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12113 LV VENT 13FR, Model Number 12113
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Perfusion Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Merge Hemo, Model RCSV2, Model/Catalog Number 99-01172-00, software versions 11.1 and 11.1.1 Product Description: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Micro Joystick R-net. Electrical wheelchair component.
High riskUsing this product could cause serious injury, illness or death — stop using it now.mo-Vis BVBA
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
Nirwana Foods, Golden Raisin, 28 oz (794g), Net Wt. 1.75 LBS, Clear Bags, 20 bags Per Case, keep at room Temperature
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nirwana Foods LLC
FDA (openFDA food enforcement)
Reported Sep 10, 2025
Orthopedic Pack, Model: 88041-12 AC2424601B 09/02/2029 Universal Pack, Model: 77165-06 AC2424902B 09/05/2029
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard Inc.
FDA (openFDA device enforcement)
Reported Sep 10, 2025Updated Aug 26, 2026
One Frozen, LLC recalls Good & Gather Frozen Burrito Bowl due to Undeclared shrimp (shellfish)
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.One Frozen, LLC
FDA (recalls & safety alerts)
Reported Sep 10, 2025
Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x, R2.x). Labeled as the following with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 10, 2025
LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
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