Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
34,943 found- Lower riskMedical device
Arrow International Inc recalls Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502
Arrow recalls pediatric catheter kits with incorrect labeling that may cause confusion in medical use. No injuries reported. Check product code AK-22502 for affected items.
ArrowJul 3, 2018 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Brilliance 16 Air, 728246 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images
Philips recalls certain Brilliance 16 Air CT scanners that may produce ring or smudge artifacts on images due to collimator compensator failure. Affected units were sold between 2018-2020.
Philips Medical SystemsJul 3, 2018 - Lower riskMedical device
Alden Optical recalls Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens
Alden Optical recalls Zenlens Toric-Gas Permeable Contact Lenses for Daily Wear in 10-cc vials due to incorrect lenses in some prescription vials. Affected vials have specific lot numbers and UDI codes.
Alden OpticalJul 3, 2018 - Lower riskMedical device
Radiometer America Inc recalls ABL800 analyzer, model numbers 393-800 and 393-801.
Radiometer recalls ABL800 analyzers (models 393-800 and 393-801) due to software causing patient demographic and test result mismatches. Affected units include specific configurations with creatinin.
RadiometerJul 3, 2018 - Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls Metformin Hydrochloride Extended Release Tablets, USP, 500 mg, packaged in a 500-count bottle, Rx only, Distributed by:
Sun Pharmaceutical recalls 500-count Metformin Hydrochloride Extended Release Tablets (NDC 62756-142-02) due to a foreign rubber glove piece found in one tablet. Consumers should check their bottles for the specific lot number.
Sun PharmaceuticalJul 3, 2018 - Lower riskDrug
Medi-Fare Drug and Home Health Center recalls Potassium Chloride For Injection Concentrate syringe 40 mEq/20 mL (2 mEq/mL), Rx only, Medi-Fare Drug Pharmaceutical
Medi-Fare recalls Potassium Chloride injection syringes with incorrect fill levels (19mL vs 20mL) that could cause unsafe potassium levels if used.
Medi-FareJul 3, 2018 - UnratedDrug
Medgyn Products, Inc. recalls Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single application vials and 12 applicators, 8 mL per box,
Medgyn Products recalls Monsel's Solution 20% (12 vials) due to failure to meet current good manufacturing practices. No specific remedy is stated in the recall notice.
Medgyn ProductsJul 3, 2018 - Lower riskFood
Byrd Cookie Co recalls PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES; NET WT. 7 OZ .(198g) BOX; BYRD COOKIE COMPANY 6700 WATERS SAVANNAH, GA
Byrd recalls pink lemonade cookies due to missing red dyes in ingredients list. Affected lots from Dec 2018 have no Red 40 or Red 3 listed.
ByrdJul 3, 2018 - Lower riskMeat & poultry
Recall Notification Report 058-2018 (Pork Products)
USDA recalls 12,946 pounds of Nueske's pork products due to misbranding. Products may contain undeclared brown rice flour and glycerin. Consumers should check labels for specific lot codes.
Nueske'sJul 2, 2018 - Use cautionVehicle
AUDI RS7 (2016) recall — Equipment
Audi is recalling 2016 RS7 vehicles with incorrect tire weight labels that could lead to vehicle overloading and increased crash risk. Owners must have the label replaced by dealers.
AudiJul 2, 2018 - Lower riskMedical device
Radiometer America Inc recalls Product: ABL800 FLEX with Crea. The ABL800 with Crea is available in the following configurations: ABL817, ABL827 and
Radiometer recalls ABL800 FLEX with Crea models (ABL817, ABL827, ABL837) due to potential underestimation of creatinine levels, which may lead to kidney issues in patients undergoing radiocontrast x-rays.
RadiometerJul 2, 2018 - Use cautionMedical device
Water Pik, Inc. recalls Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral
Water Pik recalls Sonic-Fusion Professional Model SF- 02 due to charging base overheating, which may cause fire, shock, or burns. Affected units have serial numbers SF02 17 06 01 through SF02 18 06 28.
Water PikJul 2, 2018 - Lower riskMedical device
Cypress Medical Products LLC recalls Powder Free Vinyl Exam Gloves, Item Nos. 14-116, 14-118 Product Usage: Medical exam glove for use by professional
Cypress Medical recalls powder-free vinyl exam gloves (item nos. 14-116, 14-118) due to potential failure to meet medical quality standards, risking inadequate infection protection.
Cypress MedicalJul 2, 2018 - Use cautionMedical device
Hudson Scientific LLC recalls iTOVi Tracker/Scanner, Model Nos. ITS10 and ITS15 Intended to rank galvanic skin response measurements. The results are
Hudson Scientific recalls iTOVi Tracker/Scanner models ITS10 and ITS15 due to electric shocks from improper manufacturing. Affected units have specific lot and serial numbers. Stop using immediately to avoid injury.
Hudson ScientificJul 2, 2018 - Stop using nowDrug
AuroMedics Pharma LLC recalls Piperacillin and Tazobactam for Injection USP 3.375 grams per vial, Single-Dose Vial, Rx Only. Manufactured for:
AuroMedics Pharma recalls Piperac:illin-Tazobactam injection vials with glass/silicone particles that could cause serious injury. Affected vials have specific NDC and lot numbers.
AuroMedicsJul 2, 2018 - Lower riskFood
United States Bakery Corp recalls Naked Bread Hamburger Buns #NothingToHide, 8 pack. Product is packaged in low density polyethylene bag and identified
United States Bakery Corp recalls Naked Bread Hamburger Buns #NothingToHide 8-pack due to undeclared milk. Consumers should check labels for UPC #72220 11075 and return to retailer for refund.
United States Bakery CorpJul 2, 2018 - Use cautionMeat & poultry
L&D Market, Inc. Recalls Chicken Wrap Products Due to Misbranding and Undeclared Allergens
USDA FSIS recalls L&D Market chicken wraps due to milk allergen not declared on labels. Consumers urged to discard products purchased between June 21-27, 2018.
L&D MarketJun 29, 2018 - Use cautionVehicle
SPARTAN GLADIATOR (2014) recall — Electrical System
Spartan is recalling 2010-2019 Gladiator vehicles with brittle battery cable sleeves that can arc and cause fire. Owners must have brackets installed to prevent chafing.
SpartanJun 29, 2018 - Lower riskMedical device
Luminex Corporation recalls Luminex Aries M1 System Model: Aries M6V1 Aries Software v1.0 For In Vitro Diagnostic Use in clinical laboratories.
Luminex recalls Aries M1 System software v1.0 for in vitro diagnostics due to potential patient sample mismatches and duplicate results. Affected units have specific scanner labels and were sold after April 2017.
LuminexJun 29, 2018 - Use cautionMedical device
RAYSEARCH LABORATORIES AB recalls RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),
RaySearch recalls specific versions of RayStation software for radiation therapy planning due to potential overdose risk if beam models are asymmetric. Users must verify their version and contact RaySearch for updates.
RaySearchJun 29, 2018 - Use cautionMedical device
Hitachi Medical Systems America Inc recalls Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and
Hitachi recalls Scenaria CT systems after reports of table failing to stop during patient positioning, risking injury or equipment damage. Affected units may need safety updates.
HitachiJun 29, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls 3D V, model. no. 7042042 7042059 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the
Siemens Medical recalls 3D V X-ray ceiling stands with specific model numbers due to rare risk of rope failure causing patient injury during use. Affected units may need repair or replacement.
Siemens MedicalJun 29, 2018 - Use cautionMedical device
Mevion Medical Systems, Inc. recalls MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage: Indicated for the delivery of radiation
Mevion recalls S250/Proton Beam systems with unauthorized QFix couch tops that may cause incorrect treatment or injury during radiation therapy.
MevionJun 29, 2018 - Lower riskMedical device
Quasar Bio-Tech, Inc. recalls Pure Rayz, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Quasar Bio-Tech recalls Pure Rayz Light Therapy System due to unapproved claims about collagen and elastin production. This device was not cleared by the FDA for these health claims.
Quasar Bio-TechJun 29, 2018 - Lower riskMedical device
Back 2 Basics Direct LLC recalls Dymaxeon 5.5 Curved Rod Size 5.5 x 110mm (Yellow), Model Number 06.6441B Product Usage: The Dymaxeon Spine System is
Back 2 Basics recalls Dymaxeon 5.5 Curved Rods (Model 06.6441B) that may contain 100mm rods instead of 110mm. This could cause improper spinal fixation. Affected units sold with Lot 779C4.
Back 2 BasicsJun 29, 2018 - Use cautionMedical device
Integra LifeSciences Corp. recalls MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT, Part Number A2600R The MAYFIELD¿ Infinity XR2 Base Unit is intended to be
Integra recalls MAYFIELD Infinity XR2 Base Unit adaptors (part A2600R) due to potential knob fracture during use. Affected units sold from 2018-2023; check serial numbers listed.
IntegraJun 29, 2018 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica Sample Handler Prime (SMN 11069001). The Atellica" Solution is a multi-component system for in vitro
Siemens Healthcare recalls Atellica Sample Handler Prime software version 1.13 and lower due to potential incorrect test results. Affected users should update software to fix issues with reagent locks, sample barcodes, and dilution calculations.
Siemens HealthcareJun 29, 2018 - Lower riskDrug
Fagron Compounding Services LLC dba Fagron Sterile Services recalls Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per
Fagron Sterile Services recalls Neostigmine Methylsulfate injection syringes with incorrect labeling of strength. This may cause dosing errors if used without proper verification.
Fagron Sterile ServicesJun 29, 2018 - Lower riskDrug
SCA Pharmaceuticals recalls Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total
SCA Pharmaceuticals recalls specific lots of Buffered Lidocaine 1% injection for local anesthesia due to potential stability problems affecting expiration dates. Consumers should check their lot numbers and contact the manufacturer for details.
SCA PharmaceuticalsJun 29, 2018 - Lower riskFood
May Flower International Inc. recalls 3+2 Soda Crackers (CREAM FLAVOUR)(S) packaged in a 4.4 oz, yellow package, UPC: 6 919892 633101
May Flower International recalls 3+2 Soda Crackers (Cream Flavour) due to undeclared milk content. Consumers should check for yellow 4.4oz packages with UPC 6919892633101.
May FlowerJun 29, 2018
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