FoodFeb 11, 2026
Diva Fam Sea Moss Gel Superfood recall — FDA H-0478-2026
potential Clostridium botulinum contamination
Class IIFDA: TerminatedDiva Fam Inc
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
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 categories
2026 recalls — page 107
Records are ordered by the best available source date.
FoodFeb 11, 2026
Diva Fam Sea Moss Gel Superfood recall — FDA H-0469-2026
potential Clostridium botulinum contamination
Class IIFDA: TerminatedDiva Fam Inc
FoodFeb 11, 2026
Beacon Promotions Repackaged M&Ms candies, Net Wt 1.3 oz recall — FDA H-0462-2026
Undeclared allergens (milk, soy, and peanut)
Class IIFDA: OngoingBeacon Promotions Inc
FoodFeb 11, 2026
Diva Fam Sea Moss Gel Superfood recall — FDA H-0472-2026
potential Clostridium botulinum contamination
Class IIFDA: TerminatedDiva Fam Inc
DrugFeb 11, 2026
Diclofenac Sodium, Topical Gel, 3%, 100 g tube recall — FDA D-0342-2026
Failed Viscosity Specifications: Out of Specification (OOS) [slightly lower than the limit] result in viscosity for Diclofenac Sodium Gel, 3%.
Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC
DrugFeb 11, 2026
Green Lumber Natural Fuel For Men capsule recall — FDA D-0304-2026
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
Class IFDA: OngoingGreen Lumber Holdings, LLC
DrugFeb 11, 2026
Bisoprolol Fumarate and Hydrochlorothiazide tablets, USP, 2.5 mg/6.25 mg, 100-count bottle recall — FDA D-0301-2026
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
Class IIFDA: OngoingUnichem Pharmaceuticals USA Inc.
Medical DeviceFeb 4, 2026
CareFusion 303 BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM recall — FDA Z-1217-2026
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK, Kit SKU DYNJ16826O recall — FDA Z-1198-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
NIPRO Technical Services Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011 recall — FDA Z-1185-2026
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
Class IIFDA: OngoingNIPRO Technical Services, Inc.
Medical DeviceFeb 4, 2026
Canon Medical System, USA Alphenix INFX-8000C, interventional fluoroscopic x-ray system recall — FDA Z-1176-2026
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS, Kit SKU CDS984347O recall — FDA Z-1190-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU recall — FDA Z-1192-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Broselow Pediatric Emergency Rainbow Tape recall — FDA Z-1114-2026
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Class IFDA: OngoingSunMed Holdings, LLC
Medical DeviceFeb 4, 2026
Philips Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version recall — FDA Z-1206-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) PACER / CATH LAB PACK-LF, Kit SKU recall — FDA Z-1188-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceFeb 4, 2026
Canon Medical System, USA Alphenix INFX-8000V, interventional fluoroscopic x-ray system recall — FDA Z-1179-2026
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceFeb 4, 2026
Siemens Medical Solutions USA Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T recall — FDA Z-1175-2026
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceFeb 4, 2026
Canon Medical System, USA Alphenix INFX-8000H, interventional fluoroscopic x-ray system recall — FDA Z-1178-2026
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray interventional systems may…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceFeb 4, 2026
Broselow recall — FDA Z-1117-2026
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Class IFDA: OngoingSunMed Holdings, LLC
Medical DeviceFeb 4, 2026
GOLD STAR DISTRIBUTION Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN recall — FDA Z-1181-2026
Potential exposure of rodents and rodent activity in the distribution center.
Class IIFDA: OngoingGOLD STAR DISTRIBUTION Inc.
Medical DeviceFeb 4, 2026
Broselow Domestic Complete ALS Organizer recall — FDA Z-1116-2026
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Class IFDA: OngoingSunMed Holdings, LLC
Medical DeviceFeb 4, 2026
Philips Upgrade to MR 7700 recall — FDA Z-1214-2026
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 4, 2026
Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF, Kit recall — FDA Z-1197-2026
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of…
Class IIFDA: OngoingMedline Industries, LP
About the 2026 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.