FoodFeb 11, 2026
Diva Fam Sea Moss Gel Superfood recall — FDA H-0478-2026
potential Clostridium botulinum contamination
Class IIFDA: TerminatedDiva Fam Inc
Latest records
Latest recalls — page 107
The newest recall records with useful source details are listed here.
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
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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