Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,115 results
Medical DeviceUSFDA Devices

Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

Jul 1, 2026SURGIFY MEDICAL OY
PharmaceuticalUSFDA Drugs

Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313, Telangana, India, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, NDC 31722-813-60.

Annora Pharma Private Limited
FDA DrugsClass II

Lacosamide Tablets, USP, C V, 100mg, Rx only, 60-count bottle, By: Annora Pharma Pvt., Ltd, Sangareddy -502313, Telangana, India, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, NDC 31722-813-60.

Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg.

Jul 1, 2026Annora Pharma Private Limited
Medical DeviceUSFDA Devices

Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

Jul 1, 2026SURGIFY MEDICAL OY
Medical DeviceUSFDA Devices

Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A

Philips North America Llc
FDA DevicesClass II

Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A

Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.

Jul 1, 2026Philips North America Llc
Medical DeviceUSFDA Devices

Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

Jul 1, 2026SURGIFY MEDICAL OY
PharmaceuticalUSFDA Drugs

BD ChloraPrep FREPP Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1.5 mL Applicator, 20 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-30.

CareFusion 213, LLC
FDA DrugsClass II

BD ChloraPrep FREPP Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1.5 mL Applicator, 20 Applicators, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-30.

Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area.

Jul 1, 2026CareFusion 213, LLC
Medical DeviceUSFDA Devices

Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

Jul 1, 2026SURGIFY MEDICAL OY
Medical DeviceUSFDA Devices

Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

Boston Scientific Corporation
FDA DevicesClass II

Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device

There is the potential for leakage along the drug pathway from the pump through the end of the catheter.

Jul 1, 2026Boston Scientific Corporation
Food & BeverageUSFDA Food

boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish

Boichik Bagels, Inc.
FDA FoodClass II

boichik bagels Whitefish Salad Ingredients: Smoked whitefish, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish

Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.

Jul 1, 2026Boichik Bagels, Inc.
Food & BeverageUSFDA Food

boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish

Boichik Bagels, Inc.
FDA FoodClass II

boichik bagles Tuna Salad Ingredients: albacore tuna, mayonnaise (soybean oil, water, whole eggs and egg yolks, distilled vinegar, salt, sugar, lemon juice concentrate, calcium disodium edta, natural flavors), pickle juice, mustard, chives, black pepper. Contains: Fish

Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels.

Jul 1, 2026Boichik Bagels, Inc.
Medical DeviceUSFDA Devices

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DYNJ61383C POSTERIOR SPINE PACK-LF DYNJ0843339O UPPER EXTREMITY DYNJ61907A VISCERAL ANGIOGRAM PACK-LF DYNJ0429121L

Medline Industries, LP
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DYNJ61383C POSTERIOR SPINE PACK-LF DYNJ0843339O UPPER EXTREMITY DYNJ61907A VISCERAL ANGIOGRAM PACK-LF DYNJ0429121L

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.

Jul 1, 2026Medline Industries, LP
PharmaceuticalUSFDA Drugs

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound Volume 1295 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Boston, 55 6th Rd Woburn, Massachusetts 01801-1767.

Central Admixture Pharmacy Services, Inc.
FDA DrugsClass II

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound Volume 1295 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Boston, 55 6th Rd Woburn, Massachusetts 01801-1767.

Incorrect product formulation: bag did not contain copper and famotidine per label.

Jul 1, 2026Central Admixture Pharmacy Services, Inc.
Food & BeverageUSFDA Food

Joy Rose Lassi 16 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Rose Lassi 16 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.
Food & BeverageUSFDA Food

8/9.5oz Tub Nut - Sunflower Seed

George J Howe Company, Inc.
FDA FoodClass I

8/9.5oz Tub Nut - Sunflower Seed

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Jul 1, 2026George J Howe Company, Inc.
Medical DeviceUSFDA Devices

Octopus Evolution Tissue Stabilizer, Model TS2000

Medtronic Perfusion Systems
FDA DevicesClass II

Octopus Evolution Tissue Stabilizer, Model TS2000

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

Jul 1, 2026Medtronic Perfusion Systems
PharmaceuticalUSFDA Drugs

Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.

Amgen, Inc.
FDA DrugsClass II

Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.

Presence of Foreign Substance.

Jul 1, 2026Amgen, Inc.
Food & BeverageUSFDA Food

2.0 oz Dirty Maui Onion Chip, Plastic Bag.

Utz Quality Foods, LLC
FDA FoodClass I

2.0 oz Dirty Maui Onion Chip, Plastic Bag.

Potential presence of Salmonella.

Jul 1, 2026Utz Quality Foods, LLC
Food & BeverageUSFDA Food

5# Sunflower Seeds C/NS

George J Howe Company, Inc.
FDA FoodClass I

5# Sunflower Seeds C/NS

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Jul 1, 2026George J Howe Company, Inc.
Food & BeverageFranceRappelConso

axel et paul - sorgho biologique décortiqué

axel et paul
RappelConsovolontaire (san...

axel et paul - sorgho biologique décortiqué

la teneur en zéaralénone et la somme de t-2 toxine et de ht-2 toxine

Jul 1, 2026axel et paul
Medical DeviceUSFDA Devices

Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310

PFM MEDICAL INC.
FDA DevicesClass II

Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310

A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements for in-vitro-cytotoxicity, which if in contact with a patient's vasculature could result in localized inflammation and tissue irritation.

Jul 1, 2026PFM MEDICAL INC.
PharmaceuticalUSFDA Drugs

Sensipar (cinacalcet) Tablets, 90mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks, CA 91320-1799, Made in Japan. NDC 55513-075-30

Amgen, Inc.
FDA DrugsClass II

Sensipar (cinacalcet) Tablets, 90mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks, CA 91320-1799, Made in Japan. NDC 55513-075-30

CGMP Deviations

Jul 1, 2026Amgen, Inc.
Medical DeviceUSFDA Devices

INZONE DETACHMENT SYSTEM, REF: M00345100950

Stryker Neurovascular
FDA DevicesClass II

INZONE DETACHMENT SYSTEM, REF: M00345100950

Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with an alternative technique.

Jul 1, 2026Stryker Neurovascular
Food & BeverageUSFDA Food

Joy Mango-Pina-Strawberry Lassi 16 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Mango-Pina-Strawberry Lassi 16 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.
Food & BeverageUSFDA Food

2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.

Utz Quality Foods, LLC
FDA FoodClass I

2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.

Potential presence of Salmonella.

Jul 1, 2026Utz Quality Foods, LLC

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