FoodJun 26, 2024
Heinens Heinen's Tuscan Salad Bowl Ingredients: Garbanzo recall — FDA F-1377-2024
Product contains undeclared pecans, a known allergen.
Class IIFDA: TerminatedHeinens
Latest records
Latest recalls — page 378
The newest recall records with useful source details are listed here.
FoodJun 26, 2024
Raw Farm made from unpasteurized milk, 8 oz recall — FDA F-1373-2024
Potential contamination with E. coli O157:H7
Class IFDA: TerminatedRaw Farm LLC
FoodJun 26, 2024
Clasen Quality Chocolate White Chocolate Wafer, Item # 59152 recall — FDA F-1381-2024
Potential Salmonella contamination.
Class IIFDA: TerminatedClasen Quality Chocolate Inc.
FoodJun 26, 2024
Clasen Quality Chocolate NGMO White Confectionery Wafer, Item # 60975 recall — FDA F-1382-2024
Potential Salmonella contamination.
Class IIFDA: TerminatedClasen Quality Chocolate Inc.
FoodJun 26, 2024
Clasen Quality Chocolate 1085343 10M Milk Chocolate Flavored Confectionery Drop recall — FDA F-1378-2024
Potential Salmonella contamination.
Class IIFDA: TerminatedClasen Quality Chocolate Inc.
VehicleJun 26, 2024
Frontier lower ball joint recall — NHTSA campaign 24V479000
Nissan North America, Inc. (Nissan) is recalling certain 2024 Frontier vehicles. The front right-side lower link may have been manufactured with an oversized ball joint, which can result in…
lower ball jointNissan North America, Inc.
DrugJun 26, 2024
Teva Pharmaceuticals USA Amoxicillin and Clavulanate Potassium Tablets USP, Chewable recall — FDA D-0561-2024
Subpotent Drug
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc.
DrugJun 26, 2024
Little Remedies Gas Relief Drops (Simethicone/Antigas) recall — FDA D-0557-2024
cGMP deviations: Test results confirmed aypical Burkholderia Cepacia were a result of personnel error.
Class IIFDA: TerminatedDenison Pharmaceuticals, LLC
DrugJun 26, 2024
Duloxetine Delayed-Release Capsules, USP, 60mg, 90-count bottle recall — FDA D-0562-2024
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Class IIFDA: TerminatedBreckenridge Pharmaceutical, Inc.
DrugJun 26, 2024
PURE PETROLEUM Petroleum Jelly, White Petrolatum USP, NET WT 13 OZ (368g), sold under the recall — FDA D-0560-2024
Labeling: Label Mix up; product labeled as pure white petroleum jelly actually contains petroleum jelly with Lavendar and Chamomile
Class IIFDA: TerminatedConsumer Product Partners, LLC
DrugJun 26, 2024
Dexamethasone Sodium Phosphate injection USP, 120mg per 30mL (4mg/mL), 30 mL Multiple-Dose recall — FDA D-0555-2024
Failed Impurities/Degradation Specifications: impurity sulfonic acid adduct of dexamethasone phosphate results were above spec.
Class IIFDA: OngoingEugia US LLC
DrugJun 26, 2024
MexHealth OSSOS-SANS Reforzado con: Glucosamina Curcuma Ortiga tablets recall — FDA D-0558-2024
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac and methocarbamol,
Class IIFDA: OngoingMexHealth LLC
VehicleJun 20, 2024
Volkswagen Group of front passenger recall — NHTSA campaign 24V464000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021-2024 Atlas and 2020-2024 Atlas Cross Sport vehicles. The passenger occupant detection system (PODS) may experience a…
front passengerVolkswagen Group of America, Inc.
Medical DeviceJun 19, 2024
Integra LifeSciences CODMAN EVD BACTISEAL 1.9mm I.D recall — FDA Z-2137-2024
Defect in the external sterile packaging (pouch) leading to a gap or/and weakness of the seal may compromise the product sterility.
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceJun 19, 2024
Avanos Medical NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product recall — FDA Z-2036-2024
The expiration date was not printed on the outer shipping label, leading to expired syringes being shipped to customers.
Class IIIFDA: OngoingAvanos Medical, Inc.
Medical DeviceJun 19, 2024
Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US recall — FDA Z-1921-2024
System monitor screen may display atypical behavior: Overlapping screens/buttons, Frozen screen, Distorted text, blanks, or zeroes in place of values, Unresponsive buttons where the user is…
Class IFDA: OngoingThoratec Corp.
Medical DeviceJun 19, 2024
Integra LifeSciences CODMAN BACTISEAL Clear EVD Catheter 1.9mm I.D recall — FDA Z-2138-2024
Defect in the external sterile packaging (pouch) leading to a gap or/and weakness of the seal may compromise the product sterility.
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceJun 19, 2024
Integra LifeSciences CODMAN BACTISEAL EVD Catheter Set - Indicated for gaining access to the recall — FDA Z-2136-2024
Defect in the external sterile packaging (pouch) leading to a gap or/and weakness of the seal that may compromise the product sterility.
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceJun 19, 2024
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING MyoSPECT System, Model H3912AA and H3912B, and recall — FDA Z-2040-2024
There is a potential issue regarding the service handles for the internal lead (Pb) covers in that the handles could loosen or release which could cause a cover to drop potentially…
Class IIFDA: OngoingGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
Medical DeviceJun 19, 2024
Ortho-Clinical Diagnostics VITROS Immunodiagnostic Products Anti HBs Calibrators recall — FDA Z-2142-2024
Potential for positively biased results due to signal reduction over shelf life.
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJun 19, 2024
Wondfo USA Co Independent Medical Co-op Inc., Streptococcal A rapid test kits, labeled as recall — FDA Z-2033-2024
Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home…
Class IIFDA: OngoingWondfo USA Co Ltd
Medical DeviceJun 19, 2024
Fresenius Medical Care Holdings US AquaA 900H-Typ USA-3 x 208v-Intended for the purification recall — FDA Z-2141-2024
Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard default set point range is between 4 and 18.Error message (F020104, "concentrate pressure alarm limit…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceJun 19, 2024
Wondfo USA Co Streptococcal A rapid test kits, labeled as: Wondfo Biotech Co., Ltd, WondView recall — FDA Z-2034-2024
Wondfo USA has identified unauthorized distribution of the Preview Strep A Test Kit. Unauthorized distribution of this device would include sales and distribution of this test for at-home…
Class IIFDA: OngoingWondfo USA Co Ltd
Medical DeviceJun 19, 2024
Blue Belt Technologies CORI Starter Kit, Real Intelligence CORI, CORI STARTER KIT recall — FDA Z-2135-2024
CORI Surgical System with Real Intelligence Software exhibits an increased Marker Registration Error (MRE) which may cause tracker arrays to flicker on screen of the CORI Surgical System…
Class IIFDA: OngoingBlue Belt Technologies, Inc.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories