Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,255 results
Pharmaceutical
FDA DrugsClass II

IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single d...

Lack of assurance of Sterility:

Jul 8, 2026ACCORD BIOPHARMA INC
Medical Device
FDA DevicesClass I

A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, sur...

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

Jul 8, 2026Windstone Medical Packaging, Inc.
Medical Device
FDA DevicesClass II

5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Tr...

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Jul 8, 2026Bard Access Systems, Inc.
wiseup - gant de protection multiusage
RappelConsovolontaire (san...

wiseup - gant de protection multiusage

non conforme aux normes europénnes

Jul 8, 2026wiseup
Food & Beverage
FDA FoodClass I

a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder wi...

Product may be contaminated with Clostridium botulinum.

Jul 8, 2026NARA ORGANICS INC
Pharmaceutical
FDA DrugsClass II

Cinacalcet Hydrochloride Tablets, 90 mg, 30-count bottle, Rx Only, Manufactured ...

cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).

Jul 8, 2026Cipla USA, Inc.
Medical Device
FDA DevicesClass I

Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Cat...

There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.

Jul 8, 2026Baxter Healthcare Corporation
Pharmaceutical
FDA DrugsClass II

Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Di...

Lack of Assurance of Sterility

Jul 8, 2026Asclemed USA Inc.
seablue - cube de dorade surgelé coryphene 360g
RappelConsovolontaire (san...

seablue - cube de dorade surgelé coryphene 360g

présence d'histamine supérieure au seuil règlementaire

Jul 8, 2026seablue
Medical Device
FDA DevicesClass II

Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJO...

Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.

Jul 8, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen...

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Jul 8, 2026Bard Access Systems, Inc.
Pharmaceutical
FDA DrugsClass II

BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
Pharmaceutical
FDA DrugsClass II

prednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (...

Presence of Foreign Substance

Jul 8, 2026Lupin Pharmaceuticals Inc.
Medical Device
FDA DevicesClass II

Radius VSM ECG pre-connected Set, REF: 4842, 4695

Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians away from management of true positive alarms, which could delay treatment; 2) Small and medium size blood pressure cuffs may contain rough edges, may result in skin irritation/redness.

Jul 8, 2026Masimo Corporation
Medical Device
FDA DevicesClass II

CRE Wireguided 6-8mm 240cm

Potential sterile breach of the pouches in which devices are packaged.

Jul 8, 2026Boston Scientific Corporation
Safety Alert
Health CanadaType I

Two lots of Omnitrope injectable human growth hormone recalled due to cracked ca...

Product quality

Jul 8, 2026Communications and Public Affairs Branch
Pharmaceutical
FDA DrugsClass II

BD PurPrep, (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl a...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
Pharmaceutical
FDA DrugsClass II

ChloraPrep FREPP, Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopr...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
Pharmaceutical
FDA DrugsClass II

BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v ...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) IMAGING BIOPSY TRAY, Model Number: DYNDH1068; 2)...

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Jul 8, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator...

In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.

Jul 8, 2026Accuray Incorporated
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026314 - TIFFIN

Electrical

Jul 8, 2026TC
Medical Device
FDA DevicesClass II

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotto...

Due to out-of-specification, or potential out-of-specification, levels of endotoxins

Jul 8, 2026TELEFLEX LLC
sans marque - tranche de boeuf
RappelConsovolontaire (san...

sans marque - tranche de boeuf

salmonelle

Jul 8, 2026sans marque
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