DrugJun 24, 2026
Chlorthalidone Tablets, USP, 25 mg, [100 or 1000] Tablets pr bottle recall — FDA D-0610-2026
Failed Dissolution Specifications
Class IIFDA: OngoingInventia Healthcare Limited
Latest records
Latest recalls — page 48
The newest recall records with useful source details are listed here.
DrugJun 24, 2026
Dabur India Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 recall — FDA D-0630-2026
CGMP Deviations; deficiencies observed during FDA inspection
Class IIFDA: OngoingDabur India Limited
DrugJun 24, 2026
Dabur India Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc recall — FDA D-0641-2026
CGMP Deviations; deficiencies observed during FDA inspection
Class IIFDA: OngoingDabur India Limited
DrugJun 24, 2026
Dabur India Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units recall — FDA D-0633-2026
CGMP Deviations; deficiencies observed during FDA inspection
Class IIFDA: OngoingDabur India Limited
DrugJun 24, 2026
HEALTH-TEC TOPICAL ANESTHETIC DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor recall — FDA D-0602-2026
Defective container:may contain bottles with incomplete seals
Class IIFDA: OngoingKeystone Industries
FoodJun 24, 2026
Nutrisystem Chocolate Cheesecake, 2 oz recall — FDA H-0947-2026
Undeclared Allergen (Soy)
Class IIFDA: OngoingNutrisystem Inc
FoodJun 24, 2026
Jonco Industries White Cheddar Seasoning packed in the following sizes and recall — FDA H-0953-2026
Products were made with recalled California Dairies milk powder due to Salmonella.
Class IFDA: TerminatedJonco Industries
FoodJun 24, 2026
Fairhope Roasting Company packaged in 1-gallon plastic jugs, UPC 852236006062, for food recall — FDA H-0951-2026
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement
Class IIFDA: TerminatedFairhope Roasting Company
FoodJun 24, 2026
MID DOLCIARIA SRL CANNOLI SICILIANI intended use: DESSERT condition: shelf recall — FDA H-0945-2026
The product contains unapproved colors chlorophyll E140 and E141.
Class IIFDA: OngoingMID DOLCIARIA SRL
FoodJun 24, 2026
azuma foods TAKO WASABI Seasoned Octopus with Wasabi recall — FDA H-1075-2026
Undeclared fish.
Class IFDA: OngoingAzuma Foods International Inc USA
FoodJun 24, 2026
United States Bakery Great Value Hawaiian Roll 4pk, Item # F63384 recall — FDA H-0949-2026
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
Class IIFDA: CompletedUnited States Bakery
FoodJun 24, 2026
Dkiru Adndale Magnesium Glycinate Gummies 400 mg recall — FDA H-1079-2026
Undeclared melatonin.
Class IIFDA: OngoingDkiru LLC
FoodJun 24, 2026
MID DOLCIARIA SRL .155 CRUNCHY CANNOLI GLUTEN FREE intended use: DESSERT recall — FDA H-0946-2026
The product contains unapproved colors chlorophyll E140 and E141.
Class IIFDA: OngoingMID DOLCIARIA SRL
Medical DeviceJun 17, 2026
INSPIREMD CGuard Prime Carotid Stent System, 135cm, 10mmx30mm recall — FDA Z-2329-2026
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Class IIFDA: OngoingINSPIREMD Inc
Medical DeviceJun 17, 2026
BERLIN HEART GMBH EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU recall — FDA Z-2320-2026
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
Class IIFDA: OngoingBERLIN HEART GMBH
Medical DeviceJun 17, 2026
Abbott Medical Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model recall — FDA Z-2405-2026
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
Class IIFDA: OngoingAbbott Medical
Medical DeviceJun 17, 2026
GE Medical Systems Allia IGS 7 Pulse angiographic X-ray system recall — FDA Z-2316-2026
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceJun 17, 2026
D.O.R.C. Dutch Opthalmic Research Center Intl TDC VELOCE", 25G Two Dimensional Cutter - 20k recall — FDA Z-2323-2026
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Class IIFDA: OngoingD.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Medical DeviceJun 17, 2026
ICU Medical Plum Solo Precision IV Pump, 40001-0401 recall — FDA Z-2311-2026
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceJun 17, 2026
Inter-Med Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 recall — FDA Z-2400-2026
Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most…
Class IIFDA: OngoingInter-Med Llc
Medical DeviceJun 17, 2026
CGuard Prime Carotid Stent System, 135cm, 9mx40mm recall — FDA Z-2328-2026
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Class IIFDA: OngoingINSPIREMD Inc
Medical DeviceJun 17, 2026
ICU Medical Plum Duo Infusion Pump, 40002-0401 recall — FDA Z-2312-2026
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceJun 17, 2026
INSPIREMD CGuard Prime Carotid Stent System, 135cm, 10mmx40mm recall — FDA Z-2330-2026
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Class IIFDA: OngoingINSPIREMD Inc
Medical DeviceJun 17, 2026
DT MedTech Hintermann Series Talar Implant, Left, Size 2 REF 302112 recall — FDA Z-2399-2026
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Class IIFDA: OngoingDT MedTech, LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026300 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