FoodMar 11, 2026
Juniper Granola Junebar Chocolate Cherry All Natural Snack Bar recall — FDA H-0543-2026
Products contain undeclared milk and soy.
Class IFDA: TerminatedJuniper Granola, LLC
March 2026 recalls — page 6
These records include useful source details for the selected month.
DrugMar 11, 2026
ACME UNITED 1) BZK Antiseptic Towelettes recall — FDA D-0362-2026
CGMP Deviations
Class IIFDA: OngoingACME UNITED CORPORATION
DrugMar 11, 2026
Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC recall — FDA D-0389-2026
Presence of Particulate Matter: Due to production issues
Class IIFDA: OngoingRadnostix
DrugMar 11, 2026
Nilotinib Capsules, 200 mg per capsule recall — FDA D-0382-2026
Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
Class IIIFDA: OngoingCipla USA, Inc.
DrugMar 11, 2026
Harbin Jixianglong Biotech Co Semaglutide, For Rx compounding use only recall — FDA D-0379-2026
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
Class IIFDA: OngoingHarbin Jixianglong Biotech Co., Ltd.
DrugMar 11, 2026
TEMOZOLOMIDE Product label: Temozolomide Capsules, 5mg recall — FDA D-0384-2026
Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing
Class IIFDA: OngoingRising Pharma Holding, Inc.
DrugMar 11, 2026
Harbin Jixianglong Biotech Co Semaglutide, For Rx compounding use only recall — FDA D-0380-2026
CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before distribution
Class IIFDA: OngoingHarbin Jixianglong Biotech Co., Ltd.
DrugMar 11, 2026
Nilotinib Capsules, 150 mg per capsule recall — FDA D-0381-2026
Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
Class IIIFDA: OngoingCipla USA, Inc.
Medical DeviceMar 4, 2026
Agiliti Health - Ellis Adapt Pump recall — FDA Z-1472-2026
Agiliti identified an issue where the Adapt Pump (61600200-Adapt Pump) supplied with all Adapt Line support surfaces does not re-engage the Microclimate Management function after using the…
Class IIFDA: OngoingAgiliti Health - Ellis
Medical DeviceMar 4, 2026
Medline Convenience Kits: 1) NAIL KIT recall — FDA Z-1432-2026
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 recall — FDA Z-1466-2026
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION recall — FDA Z-1433-2026
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline recall — FDA Z-1431-2026
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
EMPOWR 3D KNEE INS, 7L 16MM, VE recall — FDA Z-1459-2026
Knee and Humeral socket implants contain incorrect labeling.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 4, 2026
Medline Industries Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP recall — FDA Z-1435-2026
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Reverse Shoulder Prosthesis (RSP) RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus recall — FDA Z-1460-2026
Knee and Humeral socket implants contain incorrect labeling.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 4, 2026
Medline Industries Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING recall — FDA Z-1467-2026
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER recall — FDA Z-1463-2026
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Medline Convenience Kits: 1) NAIL KIT recall — FDA Z-1434-2026
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
Medtronic Perfusion Systems Octopus Nuvo Tissue Stabilizer, disposable tissue stabilization recall — FDA Z-1473-2026
During the manufacturing, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the…
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceMar 4, 2026
Medline Industries Convenience kits used for dialysis maintenance Medline ADD A CATH recall — FDA Z-1465-2026
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMar 4, 2026
MRIMed MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved recall — FDA Z-1436-2026
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
Class IIFDA: OngoingMRIMed Inc.
Medical DeviceMar 4, 2026
Reverse Shoulder Prosthesis (RSP) RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus recall — FDA Z-1458-2026
Knee and Humeral socket implants contain incorrect labeling.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceMar 4, 2026
Medline Industries Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG recall — FDA Z-1468-2026
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an…
Class IIFDA: OngoingMedline Industries, LP
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.