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Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026307 - GENERAL MOTORS

Steering

Jul 8, 2026TC
Medical Device
FDA DevicesClass II

SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B96...

A single lot of expired syringes were distributed due to a distribution system control failure.

Jul 8, 2026Mentor Texas LP
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

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.
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026282 - FORD

Other

Jul 8, 2026TC
Medical Device
FDA DevicesClass II

Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND ...

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

Medline Convenience Kits: 1) DYNJ0621189X, Model Number: SM RADIOLOGY-ANGIO PAC...

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.
Medical Device
FDA DevicesClass II

Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART ...

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

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

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 II

CRE Pro Wireguided 18-20mm 240cm

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

Jul 8, 2026Boston Scientific Corporation
Food & Beverage
FDA FoodClass II

Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic b...

Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)

Jul 8, 2026Fry Pie Factory LLC
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) PAIN MGMT/ PREF W. MED NDL, Model Number: PAIN0072L...

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

Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI...

Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed.

Jul 8, 2026Laborie Medical Technologies Corp
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
sans marque - tranche de boeuf
RappelConsovolontaire (san...

sans marque - tranche de boeuf

salmonelle

Jul 8, 2026sans marque
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
Vehicle
NHTSAFUEL SYSTEM, GA...

Braun Corporation - Braze Connection Missing From Fuel Line

A fuel leak increases the risk of fire.

Jul 7, 2026Braun Corporation
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026304 - BMW

Lights And Instruments

Jul 7, 2026TC
sans marque - taboulet poulet
RappelConsovolontaire (san...

sans marque - taboulet poulet

possible contamination du taboulé par la listéria

Jul 7, 2026sans marque
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026295 - ALLIANCE RV

Electrical

Jul 7, 2026TC
Safety Alert
Health CanadaClass 1

Gummy Gainz brand Protein Candy recalled due to improperly declared milk

Milk

Jul 7, 2026CFIA
Safety Alert
Health CanadaGeneral Alert

Sunluway Oven Bottom Panel Replacement recalled due to burn hazard

Burn hazard

Jul 7, 2026Consumer product safety
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