Safety Recalls
RSS ↗15,271 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 7,051–7,100 of 15,271
- Class I
Food Recall · April 23, 2025
Cinnamon Raisin Bagels: Gluten-free cinnamon raisin bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Raisins, Honey, Tapioca flour, Golden flax seDue to printing quality, label does not declare Egg allergen clearly.
- Class II
Medical Device Recall · April 23, 2025
Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.Potential breach of sterile barrier packaging.
- Class II
Medical Device Recall · April 23, 2025
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.Potential breach of sterile barrier packaging.
- Class II
Drug Recall · April 23, 2025
Lubricant Eye Drops Solution, Polyethylene Glycol 400 0.4% Eye Lubricant, Propylene Glycol 0.3% Eye Lubricant, Lubricant Eye Drops, Moisturizing, Sterile, 0.5 FL OZ (15mL) per dropper bottle, DistribucGMP deviations and lack of assurance of sterility.
- Class I
Food Recall · April 23, 2025
Multigrain Bagels: Gluten-free multigrain bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm fruit oil,Due to printing quality, label does not declare Egg allergen clearly.
- Class I
Food Recall · April 23, 2025
Brownie Chocolate Chip Cookie: Gluten-free brownie chocolate chip cookies, clear plastic bag, 4 oz, 8 cookies/package Ingredients: Sugar, Eggs, Butter, Chocolate chips, White rice flour, Cocoa powdeDue to printing quality, label does not declare these allergens clearly: Egg, Milk, Soy.
- Class I
Food Recall · April 23, 2025
Pecan Caramel Bars Individually wrapped in plastic. Ingredients: White rice flour, Sugar, Honey, Pecan pieces, Butter, Eggs, Rice milk, Potato flour, Vanilla, Baking powder, Xanthan gum, Unflavored gDue to printing quality, label does not declare these allergens clearly: Egg, Milk, Pecan.
- Class I
Food Recall · April 23, 2025
Artisan White Bread: Gluten-free artisan white bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Sugar, Palm oil, Potato flouDue to printing quality, label does not declare Egg allergen clearly.
- Class I
Food Recall · April 23, 2025
Artisan Seasoned Croutons: Gluten-free artisan seasoned croutons, vacuum-sealed clear plastic, 8 oz, bulk Ingredients: White rice flour, Water, Egg, Golden flax seed, Rice bran, Tapioca flour, HoneyDue to printing quality, label does not declare these allergens clearly: Egg and Milk.
- Class I
Food Recall · April 23, 2025
Seasoned Bread Crumbs: Gluten-free seasoned bread crumbs, vacuum-sealed clear plastic, 8 oz, bulk Ingredients: White rice flour, Water, Egg, Golden flax seed, Rice bran, Tapioca flour, Honey, Palm fDue to printing quality, label does not declare these allergens clearly: Egg and Milk.
- Class II
Medical Device Recall · April 23, 2025
MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical surgical system, Catalog Number MIRA-CAP-110, Software Version 4.0.3The MIRA Surgical System Software Version 4.0.3 loaded on the Surgeon Control Console may have the potential to exhibit interrupted motion on the display screen, caused by a software latency between the movement of the hand controllers and the movement of the Surgical Minibot arms.
- Class I
Food Recall · April 23, 2025
Coconut Macaroon Cookie: Gluten-free coconut macaroon cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: Coconut flakes, Sweetened condensed milk, Egg whites, Potato flour, Vanilla, SeDue to printing quality, label does not declare these allergens clearly: Egg, Milk, Soy.
- Class II
Medical Device Recall · April 23, 2025
Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.Potential breach of sterile barrier packaging.
- Class II
Medical Device Recall · April 23, 2025
MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.Potential breach of sterile barrier packaging.
- Class II
Medical Device Recall · April 23, 2025
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software versions 1.20A new motor/encoder and cable was introduced into instruments manufactured starting with serial number 300141 incorrectly. This incorrect installation is introducing error codes for the Dxl 9000 which prevents the assay from being performed and a delay in results from being generated, and may require field service to resolve the delay.
- Class I
Medical Device Recall · April 22, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349CAffected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
- Class II
Medical Device Recall · April 22, 2025
ICU Medical Plum Solos, Item number 400011001; infusion pumpInternal testing found that Plum Duo pumps with software version 1.1.1 have a workflow that may result in bypassing the Maximum Dose Limit alert. The Maximum Dose Limit is set in the LifeShield Drug Library Manager (DLM) within the LifeShield Medication Management Safety Software and specifies the highest dose at which the pump can be programmed for weight or BSA (body surface area) based medication rulesets. The limit can be configured for Dose, Loading Dose, and Bolus Dose.
- Class II
Drug Recall · April 22, 2025
Clindamycin HCl Capsule, 300 mg, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701. NDC#: 70518-3772-02CGMP Deviations - products manufactured in a shared facility with Ezetimibe tablets.
- Class I
Medical Device Recall · April 22, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ACCESSORY PACK SKU DYNJ59270 2. CRANI PACK-LF SKU DYNJ44805M 3. CRANIOTOMY SKU CDS982719V CDS982719W DYNJ904168FAffected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
- Class II
Medical Device Recall · April 22, 2025
ICU Medical Plum Duo, Item numbers: 1) 400020401, 2) 400021001 , and 3) 400021003; infusion pumpInternal testing found that Plum Duo pumps with software version 1.1.1 have a workflow that may result in bypassing the Maximum Dose Limit alert. The Maximum Dose Limit is set in the LifeShield Drug Library Manager (DLM) within the LifeShield Medication Management Safety Software and specifies the highest dose at which the pump can be programmed for weight or BSA (body surface area) based medication rulesets. The limit can be configured for Dose, Loading Dose, and Bolus Dose.
- Class I
Medical Device Recall · April 22, 2025
MEDLINE INDUSTRIES, LP - Northfield
Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS983611N 3. CRANIOTOMY CDS, SKU CDS983467J 4. CRANIOTOMY PACK, SKU DYNJ85807AAffected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.
- Class II
Medical Device Recall · April 22, 2025
3M Ranger Irrigation Fluid Warming Set, REF 24750Notice was issued to clarify flow rates related to the inlet fluid temperature.
- Class II
Medical Device Recall · April 22, 2025
Brand Name: Catalyst+ Product Name: C4D software used in conjunction with Catalyst (SP001-0025), Catalyst HD (SP001-0026), Catalyst PT (SP001-0027), Catalyst X4 (SP002-0035), Catalyst+Software issue with scanning equipment that can results in the filed rotation not being applied correctly.
- Class I
Medical Device Recall · April 22, 2025
Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm, 4 row); Product code VASECR35Firm has received an increase in reports regarding inadvertent instrument lockout during surgical procedures involving the device. If lockout occurs, the device will momentarily activate but will not cut or staple tissue, and additional steps will be required to open it and remove it from tissue. If user is unable to remove the device from the tissue, potential harms to patient include surgical delay, bleeding/hemorrhage, life threatening hemorrhage/hemorrhagic shock, and conversion to open therapy. Two adverse events received, including one patient death.
- Class II
Medical Device Recall · April 21, 2025
American Contract Systems, Inc.
LOWER EXTREMITY, Model: NCEX20I; LOWER EXTREMITY, Model: NCEX20J; TOTAL KNEE PACK, Model: NCTK31K; TOTAL KNEE PACK, Model: NCTK31L All convenience kits contain Specialist Blend Cast Padding, ItTest results for cast padding component included in procedure trays shows Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals exceeded residual limits, which may lead to a possible loss or lack of functionality that may lead to a delay or prolonged treatment/procedure/therapy.
- Class II
Drug Recall · April 21, 2025
Tirofiban Hydrochloride Injection 5 mg/100 mL (50 mcg/mL), 100 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520, NOut-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
- Class II
Drug Recall · April 21, 2025
Mckesson Medical-Surgical Inc. Corporate Office
EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-880-02.CGMP Deviations; potential temperature excursions due to transit delays
- Class II
Medical Device Recall · April 21, 2025
Becton Dickinson Infusion Therapy Systems, Inc.
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter 20GX1.00IN STRAIGHT BC, REF: 386803; BD Cathena Safety IV Catheter BD MultiguarDue to a manufacturing defect IV catheter may have a hole in the septum, which may result in blood leakage from the septum during insertion, which may cause blood exposure or the need for a second IV to be placed - which may result in therapy delay.
- Class II
Drug Recall · April 21, 2025
Mckesson Medical-Surgical Inc. Corporate Office
PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21CGMP Deviations; potential temperature excursions due to transit delays
- Class II
Medical Device Recall · April 21, 2025
BIB Balloon in Balloon Dilatation Catheter. Model Number: 420Balloon extension lumens are not printed correctly. Specifically, the inner balloon inflation hub was labeled as the outer balloon, and the outer balloon inflation hub was labeled as the inner balloon.
- Class II
Medical Device Recall · April 21, 2025
Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide MonitorSampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO) monitor may have residual carbon monoxide and volatile organic compounds present due to insufficient aeration of the cannula's carbon filter prior to sealing, which may lead to higher than expected ETOCc scores during clinical evaluations.
- Class II
Drug Recall · April 21, 2025
Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL), 250 mL single-dose container (bag), Rx only, Manufactured in India for: Eugia U.S. LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520Out-of-Specification test results were obtained in at long term conditions during 3 month's stability study for related substances.
- Class II
Drug Recall · April 21, 2025
Mckesson Medical-Surgical Inc. Corporate Office
BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK.CGMP Deviations; potential temperature excursions due to transit delays
- Class I
Food Recall · April 21, 2025
Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe Springs, CA 90670 USA; UPC# 8 94042 00256 2Undeclared allergen ingredient (milk)
- Class II
Food Recall · April 19, 2025
Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923820. Made in USA.Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Class II
Food Recall · April 19, 2025
Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923813. Made in USA.Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Class II
Food Recall · April 19, 2025
Item M0053, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN* 50195500004896. Made in USA.Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Class II
Food Recall · April 19, 2025
Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW Formed Oval 6/3.5LB bags per case. GTIN*10044979922687. Made in USA.Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
- Class II
Drug Recall · April 18, 2025
niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, Mfd for: Civica, Inc., Lehi, UT 84043,Mfd by: American Regent, Inc., New Albany, OH 43064. NDC CartoLack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
- Class II
Drug Recall · April 18, 2025
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 10mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New JersDefective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
- Class II
Drug Recall · April 18, 2025
niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 mL Single Dose Vial, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC carton: 0517-0735-10 / NDC Vial: 0517-0735-01]Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
- Class II
Drug Recall · April 18, 2025
Preferred Pharmaceuticals, Inc.
Clindamycin Hydrochloride Capsules, USP, 300mg, 30-count bottles, Manufactured by: Glenmark Pharmaceuticals Limited, NDC 68788-8685-03.cGMP Deviations
- Class II
Food Recall · April 17, 2025
Mens Room Roasted Red Salsa is refrigerated product, packaged in Polypropylene container, net wt. 13 oz, UPC 1 18738 00999. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class II
Medical Device Recall · April 17, 2025
Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN MWCE-18S-3/2-TORNADO (GPN G08261), RPN MWCE-18S-3/2-Cook Medical identified that devices from the affected device lots may contain the incorrectly sized embolization coil.
- Class II
Food Recall · April 17, 2025
Medium Salsa Costco item, is refrigerated product and packaged in Polypropylene container, net wt. 32 oz, UPC 1 18738 01016. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class II
Medical Device Recall · April 17, 2025
Check=Flo Performer Introducer, 10.0Fr, Reference Part Number(RPN) REF RCFW-10.0-0-38-30-RB, Order Number (GPN) REF G08686,Cook Medical identified that devices from the affected device lots may contain the incorrectly sized introducer sheath.
- Class II
Food Recall · April 17, 2025
Verde Salsa is refrigerated product, packaged in Polypropylene container, net wt. 12.5 oz, UPC 1 18738 03719. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class I
Drug Recall · April 17, 2025
Ropivacaine Hydrochloride Injection, USP, 0.5%, 500 mg per 100 mL (5mg/mL), Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Mehsana, India, , Distributed by: Amneal Pharmaceuticals LLC, BridgewatePresence of Particulate Matter
- Class II
Food Recall · April 17, 2025
Traditional Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54636. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.comSalsa products are recalled due to potential contamination with wood particles.
- Class II
Medical Device Recall · April 17, 2025
Check=Flo Performer Introducer, 14.0Fr, Reference Part Number(RPN) REF RCFW-14.0-0-38-30-RB, Order Number (GPN) REF G08957,Cook Medical identified that devices from the affected device lots may contain the incorrectly sized introducer sheath.