FoodMay 21, 2025
Knockroe Bonya Mango Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0766-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 106
Records are ordered by the best available source date.
FoodMay 21, 2025
Knockroe Bonya Blueberry Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0765-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Knockroe Bonya Strawberry Yogurt Parfait, 8oz, Plastic cups with recall — FDA F-0763-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Knockroe Bonya Coconut Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0771-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Bondsforever, Inc dba Shastha Foods Dixit Foods, Pohe, Net Wt recall — FDA F-0809-2025
Undeclared allergens (milk and/or peanuts).
Class IIFDA: OngoingBondsforever, Inc dba Shastha Foods
FoodMay 21, 2025
Knockroe Bonya Black Cherry Yogurt Parfait, 8oz, Plastic cups with recall — FDA F-0774-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Knockroe Bonya Pineapple Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0770-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Ray & Mascari Tomatoes, retail 4 Count Vine Ripe Tomatoes packaged in clam recall — FDA F-0776-2025
Potential Contamination of Salmonella.
Class IFDA: TerminatedRay & Mascari, Inc.
FoodMay 21, 2025
Knockroe Bonya Lemon Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0768-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Hanshaw & Capling Farms H&C Farms Raw Premium Tomatoes, Naturally Grown from Seed Net recall — FDA F-0775-2025
Potential Salmonella Contamination
Class IFDA: TerminatedHanshaw & Capling Farms, LLC
FoodMay 21, 2025
Knockroe Bonya Passion Fruit Yogurt Parfait, 8oz, Plastic cups with recall — FDA F-0772-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Knockroe Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0767-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
FoodMay 21, 2025
Knockroe Bonya Raspberry Yogurt Parfait, 8oz, Plastic cups with plastic recall — FDA F-0769-2025
Undeclared Almonds
Class IFDA: TerminatedKnockroe Inc.
VehicleMay 21, 2025
Ram ProMaster camera recall — NHTSA campaign 25V330000
Chrysler (FCA US, LLC) is recalling certain 2022-2025 Ram ProMaster vehicles. A software error in the security gateway module may cause the rearview camera image not to display. As such,…
cameraChrysler (FCA US, LLC)
DrugMay 21, 2025
Empower Clinic Services, LLC dba Empower Testosterone Cypionate Injection, 200 mg/mL, CIII recall — FDA D-0420-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingEmpower Clinic Services, LLC dba Empower Pharmacy
DrugMay 21, 2025
L'Oreal USA La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne recall — FDA D-0417-2025
Chemical Contamination: This recall has been initiated due to detected trace levels of benzene.
Class IIFDA: OngoingL'Oreal USA
DrugMay 21, 2025
L'Oreal USA La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 recall — FDA D-0418-2025
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm…
Class IIFDA: OngoingL'Oreal USA
DrugMay 21, 2025
L'Oreal USA La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne recall — FDA D-0419-2025
cGMP Deviations: The recall was initiated due to detected trace levels of benzene in a specific lot of this product lot (MYX46W), however out of an abundance of caution, the firm…
Class IIFDA: OngoingL'Oreal USA
Medical DeviceMay 14, 2025
GALT Centeze Catheter REF: DRC-002-05 DRC-002-06 The Centeze is intended for use in recall — FDA Z-1731-2025
Due to a potential open seal in the sterile barrier packaging .
Class IIFDA: OngoingGalt Medical Corporation
Medical DeviceMay 14, 2025
Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set recall — FDA Z-1723-2025
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back…
Class IIFDA: OngoingAmbu Inc.
Medical DeviceMay 14, 2025
Bausch & Lomb Surgical Intraocular lens. enVista Monofocal IOL, All models starting with EE recall — FDA Z-1679-2025
In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista…
Class IFDA: OngoingBausch & Lomb Surgical, Inc.
Medical DeviceMay 14, 2025
Galt Medical Introducer Kit- Coaxial Dilator REF: KIT-002-28, 00841268104730 KIT-002-34 recall — FDA Z-1735-2025
Due to a potential open seal in the sterile barrier packaging.
Class IIFDA: OngoingGalt Medical Corporation
Medical DeviceMay 14, 2025
Integra LifeSciences CODMAN Disposable Perforator, 14mm recall — FDA Z-1716-2025
Inadequate weld that can potentially cause the product to disassemble.
Class IFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Medical DeviceMay 14, 2025
Galt Medical Introducer Needle REF NDL-107-04 These needles are used for the percutaneous recall — FDA Z-1736-2025
Due to a potential open seal in the sterile barrier packaging.
Class IIFDA: OngoingGalt Medical Corporation
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.