Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,255 results
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY, Model Number: PAIN16...

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

Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with the belo...

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

Jul 8, 2026DEPUY (IRELAND)
Safety Alert
Health CanadaType II

Alice Le System - Sleepware Software

Unauthorised device

Jul 8, 2026Medical devices
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
Pharmaceutical
FDA DrugsNot Yet Classified

Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection USP, 1mg per ...

CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

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

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

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
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
Food & Beverage
FDA FoodClass II

Ocular Plus with Lutein, Zeaxanthin, and Omega 3-6-9; Dietary Supplement, 200 Ca...

Dietary supplement product Ocular Plus contains undeclared Yellow#5.

Jul 8, 2026Provision Health Corp. dba PH Labs
Medical Device
FDA DevicesClass II

CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ...

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

Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Sy...

Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.

Jul 8, 2026Zimmer Surgical Inc
Medical Device
FDA DevicesClass II

CRE Wireguided 18-20mm 240cm

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

Jul 8, 2026Boston Scientific Corporation
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 II

CRE Wireguided 15-18mm 240cm

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

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

CRE Wireguided 12-15mm 240cm

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

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

Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590

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

Accucaine, Kit contains: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single...

Lack of Assurance of Sterility

Jul 8, 2026Asclemed USA Inc.
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

CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 ...

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

CRE Pro Wireguided 12-15mm 240cm

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

Jul 8, 2026Boston Scientific Corporation
Pharmaceutical
FDA DrugsClass II

Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only,...

Subpotent Drug

Jul 8, 2026ACCORD HEALTHCARE, INC.
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026293 - WINNEBAGO INDUSTRIES

Label

Jul 8, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026280 - FORD

Powertrain

Jul 8, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026292 - LAND ROVER

Airbag

Jul 8, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026281 - FORD

Powertrain

Jul 8, 2026TC
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