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wiseup - gant de protection multiusage
RappelConsovolontaire (san...

wiseup - gant de protection multiusage

non conforme aux normes europénnes

Jul 8, 2026wiseup
pas de marque. - herbes épices bbq
RappelConsovolontaire (san...

pas de marque. - herbes épices bbq

résidus de pesticides.

Jul 8, 2026pas de marque.
Food & Beverage
FDA FoodClass II

MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage ...

Potential contamination with plastic material

Jul 8, 2026MARS SNACKING
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
Medical Device
FDA DevicesClass I

Medtronic Harmony Delivery Catheter System

Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under certain procedural or anatomical conditions due to a manufacturing issue.

Jul 8, 2026Medtronic Heart Valves Division
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) MULTIMED, 7FR, 20CM, 3L, CVC BUNDLE, Model Number:...

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
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
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.
Vehicle
NHTSAELECTRICAL SYSTEM

BMW of North America, LLC - Park Outside: Engine Starter May Corrode and Overhea...

A short circuit in the starter relay may increase the risk of a fire.

Jul 8, 2026BMW of North America, LLC
Pharmaceutical
FDA DrugsClass II

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

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

Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below...

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

Jul 8, 2026DEPUY (IRELAND)
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
Medical Device
FDA DevicesClass II

CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 ...

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.
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE, Model Number: AR...

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
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

CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 ...

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.
Medical Device
FDA DevicesClass I

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

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
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026282 - FORD

Other

Jul 8, 2026TC
Medical Device
FDA DevicesClass II

5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI ...

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.
Medical Device
FDA DevicesClass II

RayCare 2024A SP1. Oncology Information Systems.

Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.

Jul 8, 2026RAYSEARCH LABORATORIES AB
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM, Model Number: ECVC8520; ...

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

CRE Pro Wireguided 6-8mm 240cm

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

Jul 8, 2026Boston Scientific Corporation
Medical Device
FDA DevicesClass II

CRE Wireguided 8-10mm 240cm

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

Jul 8, 2026Boston Scientific Corporation
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