Food & Beverages
HIGH
FDA FOOD
Mangalm Tops GOLD Khatta Meetha Pickle Recalled Over Erucic Acid Adulteration (480 Cans, 2026)
Potential adulteration with erucic acid from mustard oil ingredient.
Mangalm
Potential adulteration
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. Screw System Recalled for MRI Heating Risk in 5,568 Units (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS GmbH Recalled 510 I.T.S Straight Plate with Angular Stability Over MRI Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. GmbH LRS Orthopedic System Recall: 176 Units for MRI Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. Volar Radius Plate PROlock II Recall 220 Units for MRI Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS GmbH Recalled 11 Pelvic Reconstruction System PRS Components for MRI Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS GmbH Pilon Plate with Angular Stability Recalled for MRI Heating Risk (2026) 101 Units
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. FR.O.H. Calcaneus Plate Recalled for MRI Heating Risk in 4 Units (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS Fibula Plate PROlock with Angular Stability Recall Affects 869 Units (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. GmbH Claviculaplate with Angular Stability Recalled for MRI Heating Risk 322 Units (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. GmbH Distal Humeral Plates Recalled for MRI Heating Risk — 12,059 Units (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. Pelvic Reconstruction System Recall for MRI Heating Risk (46,637 Units) 2026
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. GmbH Recalls 15,517 FLS Foot Locking Plates System and Hallux Osteotomy Plates Over MRI Heat‑
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS Recalls 70 Olecranon Plates Over MRI RF Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS GmbH Recalls 623 HCS Headless Cannulated Screws Over MRI Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS GmbH HLS Hand Locking Plates System Recalled for MRI Heating Risk (1,307 Units, 2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
ITS GmbH Humeral Head Plate MRI Recall Affects 292 Units in 2026
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
I.T.S. Ulna Locking Plate Systems Recalled Over MRI Heating Risk (2026)
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
I.T.S. GmbH
Updated MRI
Health & Personal Care
HIGH
FDA DEVICE
Datascope CS100 IABP Recall 2026: 10,897 Devices for Battery Runtime Update
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
Datascope
The firm
Health & Personal Care
HIGH
FDA DEVICE
Datascope CS300 IABP Recall 2026 Aims to Update IFU Battery Specs (10897 Units Worldwide)
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
Datascope
The firm