Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,256 results
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
Food & Beverage
FDA FoodClass II

MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net ...

Potential contamination with plastic material

Jul 8, 2026MARS SNACKING
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026281 - FORD

Powertrain

Jul 8, 2026TC
Medical Device
FDA DevicesClass II

Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESI...

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 I

Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401...

Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge during use and contact circulating blood or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.

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

CRE Wireguided 10-12mm 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

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 - 2026280 - FORD

Powertrain

Jul 8, 2026TC
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 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

Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT 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
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
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 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

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

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
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026293 - WINNEBAGO INDUSTRIES

Label

Jul 8, 2026TC
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO, Model Number: DYNJ57922A

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
Food & Beverage
FDA FoodClass I

FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGRE...

Undeclared peanuts.

Jul 8, 2026Western Mixers Produce & Nuts, Inc.
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
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)
Medical Device
FDA DevicesClass II

Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS ...

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) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TU...

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
← PreviousPage 8 of 3,011Next →