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
35,004 found- Use cautionVehicle
CRUISE CAR MOKE (2019) recall — Visibility
Cruise Car is recalling 2019 Moke vehicles with potentially unsafe windshields that could reduce driver visibility and increase crash risk. Owners will receive free windshield replacements.
Cruise CarDec 18, 2019 - Use cautionVehicle
FOREST RIVER GEORGETOWN (2020) recall — Trailer Hitches
Forest River is recalling 2020 Georgetown motorhomes with potentially loose trailer hitch bolts that could cause detachment during towing, increasing crash risk. Owners should contact customer service for free tightening.
Forest RiverDec 18, 2019 - Use cautionVehicle
FORD F-150 (2020) recall — Tires
Ford is recalling 2020 F-150 trucks with damaged 17-inch spare tires that may rapidly lose air pressure or detach, increasing crash risk. Owners will receive free tire replacements.
FordDec 18, 2019 - Use cautionMedical device
Elekta, Inc. recalls Elekta Unity, Image-Guided Radiation Therapy System
Elekta recalls specific Unity radiation therapy systems due to reported excessive heating in the MRL Gradient Connection Module. Affected units have serial numbers starting with 600014 to 600035. Contact Elekta for details.
ElektaDec 18, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista Enzymatic Creatinine (ECREA) reagent, SMN 10700444
Siemens Healthcare recalls Dimension Vista Enzymatic Creatinine reagent (SMN 10700444) due to potential false low creatinine results for patients on phenindione therapy. All lots affected.
Siemens HealthcareDec 18, 2019 - Lower riskMedical device
Covidien LLC recalls Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10, Item Code SL1625G - Product Usage: Indicated for use in soft
Covidien recalls specific Polysorb suture lots due to potential packaging issues that could affect humidity or sterility. Affected items may not be safe for surgery.
CovidienDec 18, 2019 - Use cautionDrug
MPRX, Inc. dba Medical Park Pharmacy recalls Squaric Acid 0.1% Topical Solution (Clinic) 30 mL
Medical Park Pharmacy recalls Squaric Acid 0.1% Topical Solution due to incorrect labeling and use of expired components.
Medical Park PharmacyDec 18, 2019 - Lower riskFood
Northwest Gourmet Food Products Inc recalls Smoked Salmon Chowder, Pike Place Chowder brand, item #89201, distributed By PPC Trading Co. M. BOX #262 4580 Klahanie
Northwest Gourmet recalls Smoked Salmon Chowder due to gluten-free packaging mislabeling. The outer package claims gluten-free but inner pouch contains wheat. Consumers should check for wheat in the pouch label.
Northwest GourmetDec 18, 2019 - Stop using nowConsumer product
Hillsdale Furniture Recalls Five-Drawer Chests Due to Tip-Over and Entrapment Hazards
Hillsdale Furniture recalls five-drawer chests due to instability and tip-over risks that can cause serious injury or death to children. Consumers must anchor chests to walls or return for repair/refund.
Hillsdale FurnitureDec 18, 2019 - Use cautionVehicle
OLIVER TRAVEL TRAILERS LEGACY ELITE II (2019) recall — Suspension
Oliver recalls 2017-2019 Legacy Elite II travel trailers with potentially improperly tightened axle bolts, risking brake failure or wheel detachment. Owners must contact for free retorquing.
OliverDec 17, 2019 - Lower riskMedical device
Boston Scientific Corporation recalls AMS 700 100 mL, Spherical Reservoir with InhibiZone, Part No. 72404156 - Product Usage: intended for use in the
Boston Scientific recalls AMS 700 100mL Spherical Reservoir with InhibiZone due to incorrect labeling. This may cause confusion with different product types. Consumers should check labels and contact the company for clarification.
Boston ScientificDec 17, 2019 - Lower riskMedical device
W L Gore & Associates, Inc. recalls Conformable Thoracic Stent Graft, Rx only, Sterile EO - Product Usage: This device is intended for endovascular repair
W L Gore recalls specific Conformable Thoracic Stent Graft models with incorrect labeling that could lead to improper use. Affected units have serial numbers 21225065-21225084.
W L GoreDec 17, 2019 - Lower riskMedical device
Arthrex, Inc. recalls Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Arthrex recalls reusable non-sterile Fibulock Fibular Nail Instrument Set with batch 051838 due to potential hub attachment tube blockage. Affected users should contact Arthrex for details.
ArthrexDec 17, 2019 - Lower riskMedical device
Vitreq Bv recalls VitreQ 23G Pick Needles-REF: CN23.D04 GTIN: 8719214221584
Vitreq recalls all 23G Pick Needles (GTIN: 8719214221584) due to potential pouch tears compromising sterility. No remedy specified in official notice.
VitreqDec 17, 2019 - Use cautionMedical device
Quest Medical, Inc. recalls Ref 801168, MPS Top Cover Replacement Kit, 1 UNITS, UDI: (01)2 0634624 81168 7 (11)190916 (17)290913 (10)059135 (The
Quest Medical recalls 1 unit of MPS Top Cover Replacement Kit (UDI: 01)2 0634624 81168 7) due to potential potassium overdelivery during open heart surgery. Affected units may require medical intervention.
Quest MedicalDec 17, 2019 - Stop using nowDrug
Hikma Pharmaceuticals USA Inc. recalls Ketorolac Tromethamine Injection, USP 60 mg/2 mL (30 mg/mL), packaged in 2 mL Single Dose Vials (NDC 0641-6043-01), 25
Hikma Pharmaceuticals recalls Ketorolac injection vials with polydimethylsiloxane particles. Stop using if you have these specific vials. No remedy provided in official notice.
Hikma PharmaceuticalsDec 17, 2019 - Stop using nowDrug
Motto International Corp recalls Bull Platinum 30000 Capsules, 1000 mg, in orange, white, yellow background with silver text, packaged in 2, 4 and 10
Motto International recalls Bull Platinum 30000 capsules because they contain undeclared tadalafil and lack FDA approval. Check your bottle if you bought them in Texas.
Bull PlatinumDec 17, 2019 - UnratedDrug
Glenmark Pharmaceuticals Inc., USA recalls Glenmark Ranitidine Tablets USP 300 mg Rx Only 250 Tablets Manufactured by: Glenmark Pharmaceuticals Ltd.
Glenmark Pharmaceuticals recalls 300 mg ranitidine tablets due to detected NDMA impurity. This may pose health risks. Consumers should check NDC numbers and contact the company for details.
GlenmarkDec 17, 2019 - Stop using nowFood
TFI Holding dba Grey Ghost Bakery recalls GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152
Grey Ghost Bakery recalls lemon sugar scratch-made cookies due to undeclared sulfites. Check UPCs and lot codes if you have these products.
Grey Ghost BakeryDec 17, 2019 - Use cautionConsumer product
J. Crew Recalls Boys' Denim Pants Due to Aspiration and Choking Hazards
J. Crew recalls boys' stone washed denim pants sold in Pakistan with small stones that can cause choking or aspiration in young children. Remove stones from pockets or waistband to eliminate hazard.
J. CrewDec 17, 2019 - Use cautionVehicle
MACK ANTHEM (AN) (2020) recall — Steering
Mack is recalling 2020 Anthem trucks with potential steering drag link separation. If the drag link separates, loss of steering control may cause a crash. Owners should contact Mack for free repairs.
MackDec 16, 2019 - Use cautionVehicle
FORETRAVEL REALM (2020) recall — Service Brakes
Foretravel is recalling 2020 Realm vehicles with potential air brake valve issues that could increase stopping distance, risking crashes. Owners must contact Foretravel for free valve replacement.
ForetravelDec 16, 2019 - Lower riskMedical device
Nextremity Solutions recalls Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot
Nextremity Solutions recalls Stratum Lapidus Plate (Part No. STRM-LAP-SMR) due to incorrect plate type. This could cause improper bone fixation. Affected units have UDI 00817701025467.
Nextremity SolutionsDec 16, 2019 - Lower riskMedical device
Ortho Clinical Diagnostics Inc recalls VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and
Ortho Clinical Diagnostics recalls VITROS Chemistry Calibrator Kit 2 for VITROS 250/350/5,1 FS/4600/XT 3400 systems. This kit may cause inaccurate sodium results in urine tests. Affected lots include 277 (Dec 2019), 288 (May 2020), 298 (Nov 2020), and 219 (Jul 2021).
Ortho Clinical DiagnosticsDec 16, 2019 - Lower riskMedical device
Smith & Nephew, Inc. recalls LEGION AP Cutting Block Size 4, REF 71434409; LEGION AP Cutting Block Size 6, REF 71434411; LEGION AP Cutting Block
Smith & Nephew recalls certain LEGION AP Cutting Blocks with oversize green plunger holes that may not meet design specs. Affected units include sizes 4, 6, 7, and 8 with specific lot numbers.
Smith & NephewDec 16, 2019 - Lower riskMedical device
Microbiologics Inc recalls Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used
Microbiologics recalls Gram-Positive Blood Culture Control Panels (Catalog #8180) due to incorrect hydration fluid specification. This may affect test accuracy in medical labs. No immediate action needed but verify your product model.
MicrobiologicsDec 16, 2019 - Lower riskMedical device
GE Healthcare, LLC recalls Centricity Universal Viewer 6.0, a device that displays medical images and data from various imaging sources, and from
GE Healthcare recalls Centricity Universal Viewer 6.0 SP10+ due to potential misdiagnosis from incorrect grayscale measurements in images with varying pixel sizes. Affected units may require correction to ensure accurate medical imaging.
GE HealthcareDec 16, 2019 - Use cautionMedical device
Synthes, Inc. recalls 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE, Part Number 04.210.118TS - Product Usage:Sterile Tube Packaging is a
Synthes recalls sterile tube packaging with a possible risk of surgical delay if inner cap opens during use. Affected units include specific lot numbers.
SynthesDec 16, 2019 - Use cautionDrug
Akorn Inc recalls Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL dropper bottle, Rx only, HI-TECH PHARMACAL CO., INC.,
Akorn recalls 16,078 bottles of Hydrocortisone and Acetic Acid Otic Solution due to subpotent drug levels. Check your lot number.
AkornDec 16, 2019 - Lower riskDrug
Pharmedium Services, LLC recalls NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex
PharMEDium Services recalls specific NORepinephrine Bitartrate 500mL Dextrose injections with subpotent drug levels. This may cause ineffective treatment. Check lot numbers on the product label for affected batches.
PharMEDiumDec 16, 2019
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