Health & Personal Care Recalls

1,620 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH Claviculaplate with Angular Stability Recalled for MRI Heating Risk 322 Units (2026)

I.T.S. GmbH recalled 322 Claviculaplate with Angular Stability devices sold nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than the IFU reflected. Healthcare providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH Distal Humeral Plates Recalled for MRI Heating Risk — 12,059 Units (2026)

I.T.S. GmbH recalled 12,059 Distal Humeral Plates with Angular Stability due to MRI heating risk. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than reflected in the IFU. Healthcare providers and patients should stop using the device and follow recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Pelvic Reconstruction System Recall for MRI Heating Risk (46,637 Units) 2026

I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.

I.T.S. GmbH
Updated MRI
Read more
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‑

I.T.S. GmbH recalled 15,517 FLS Foot Locking Plates System and HOL Hallux Osteotomy locking plates distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than previously reflected in the IFU. Patients and healthcare providers should stop using this device immediately and follow the recall instructions from:

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS Recalls 70 Olecranon Plates Over MRI RF Heating Risk (2026)

ITS recalls 70 Olecranon Plates with Angular Stability distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using this device immediately and contact ITS or their healthcare provider for instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Recalls 623 HCS Headless Cannulated Screws Over MRI Heating Risk (2026)

ITS GmbH recalled 623 HCS Headless Cannulated Screws distributed nationwide to U.S. healthcare facilities. The defect involves higher RF-induced temperature increases during certain MRI procedures than the IFU described. Affected patients and providers should stop using immediately and follow recall instructions. Contact ITS GmbH or your healthcare provider for instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH HLS Hand Locking Plates System Recalled for MRI Heating Risk (1,307 Units, 2026)

ITS GmbH recalled 1,307 units of the HLS Hand Locking Plates System distributed nationwide in the United States after MRI safety testing showed higher RF-induced temperature increases. The issue exceeds what is described in the IFU under certain MRI conditions. Patients and healthcare providers should stop using the device immediately and follow ITS GmbH's recall instructions.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Humeral Head Plate MRI Recall Affects 292 Units in 2026

ITS GmbH recalled 292 proximal humeral plates nationwide in the United States after MRI safety testing showed higher RF-induced heating under certain MRI conditions. The heating can occur during MRI and may cause burns or tissue damage. Patients and clinicians should stop using the device immediately and follow the recall instructions from ITS GmbH and their healthcare providers.

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Ulna Locking Plate Systems Recalled Over MRI Heating Risk (2026)

I.T.S. GmbH recalled 120 units of its DUL and UOL ulna locking plate systems distributed nationwide to U.S. healthcare providers after MRI safety testing showed higher RF-induced heating. The updated testing found temperature increases under certain MRI conditions not reflected in the Instructions for Use. Healthcare facilities and patients should stop using the devices immediately and follow the厂

I.T.S. GmbH
Updated MRI
Read more
Health & Personal Care
HIGH
FDA DEVICE

Datascope CS300 IABP Recall 2026 Aims to Update IFU Battery Specs (10897 Units Worldwide)

Datascope Corp. recalls 10,897 CS300 IABP devices sold through healthcare providers worldwide after determining the battery runtime and cycle specifications in the Instructions for Use must be updated. The issue is an information update rather than a device fault. Stop using the device immediately and follow the manufacturer’s recall instructions. Contact Datascope Corp. or your healthcare team to

Datascope
The firm
Read more
Recalled Iristar Minoxidil Spray Bottles with packaging
HIGH
CPSC

Iristar Minoxidil Spray Recalled Over Child Poisoning Risk

Iristar recalled Minoxidil Spray Bottles on January 22, 2026, due to a serious poisoning risk to children. The product fails to meet child-resistant packaging standards mandated by the Poison Prevention Packaging Act. Consumers should stop using the product immediately and secure it out of children's reach.

Shaoshan Leiluo Trading Co., Ltd. of Shaoshan, Hunan of China
The recalled
Read more
Health & Personal Care
HIGH
FDA DRUG

Unichem Pharmaceuticals Recalls Bisoprolol Tablets Over Impurity Risk

Unichem Pharmaceuticals recalled Bisoprolol Fumarate and Hydrochlorothiazide tablets on January 21, 2026. The recall affects tablets that do not meet impurity specifications for N-Nitroso Bisoprolol. Consumers should stop using the product and contact their healthcare provider immediately.

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
cGMP Deviations:
Read more
Health & Personal Care
HIGH
FDA DEVICE

Stryker Recalls MOLLI 2 Surgical Markers Over Dislodging Risk

Stryker recalled 5,864 units of the MOLLI 2 surgical markers on January 21, 2026. The recall follows concerns that magnetic surgical tools may dislodge markers during procedures. Healthcare providers and patients must stop using these devices immediately.

Stryker
Due to
Read more
Health & Personal Care
HIGH
FDA DEVICE

STAAR Surgical AG EVO+ Visian TICL VTICM5 Recalled for 12.6 mm Length Mismatch (2026)

STAAR Surgical AG recalled 7 EVO+ Visian TICL VTICM5 lenses after finding a labeling error that listed 12.1 mm length but which are 12.6 mm. The mismatch can cause excessive vault and ocular complications. Physicians and patients should stop using the device immediately and follow manufacturer instructions for recall actions.

STAAR Surgical AG
Toric Implantable
Read more
Health & Personal Care
HIGH
FDA DEVICE

Auris Health Recalls Bronchoscopy Device Over Software Issue

Auris Health recalled 173 bronchoscopy devices due to a software malfunction. This issue could lead to improper robotic arm positioning, risking patient safety. The recall affects devices distributed nationwide and in Canada, with the announcement made on January 21, 2026.

Auris Health
Device for
Read more
Health & Personal Care
HIGH
FDA DRUG

Unichem Pharmaceuticals Recalls Doxazosin Tablets Over ID Error

Unichem Pharmaceuticals recalled 60,000 bottles of Doxazosin Tablets on January 21, 2026. The tablets were imprinted with the wrong ID, posing a serious risk to consumers. Healthcare providers and users should stop using the product immediately.

DOXAZOSIN MESYLATE
Tablets/Capsules Imprinted
Read more
Health & Personal Care
HIGH
FDA DEVICE

Agiliti Recalls Adapt Pump Over Microclimate Management Failure

Agiliti Health recalled 4,286 Adapt Pumps on January 21, 2026, after identifying a malfunction. The issue prevents the Microclimate Management function from re-engaging following the Autofirm function. This defect poses a risk to patients relying on the device for safe pressure management.

Agiliti Health - Ellis
Agiliti identified
Read more
Health & Personal Care
HIGH
FDA DRUG

Acme United MED NAP BZK Antiseptic Towelettes Recalled in 2026 (100-Count)

Acme United Corporation recalled Med Nap BZK Antiseptic Towelettes, 100-count, distributed nationwide. The FDA-listed CGMP deviations raise concerns about manufacturing quality and product safety. Consumers and healthcare providers should stop using the product and follow the recall letter for guidance.

Acme United Corporation
CGMP Deviations
Read more
Previous
12345...81
Next

Related Categories

Food & BeveragesVehicles & PartsToys & Children's ProductsFurnitureBaby ProductsElectronicsTools & HardwareHome & Garden

Category Statistics

Total Recalls
1,620
Pages
81