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
34,956 found- Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Electrical System
Daimler Trucks North America recalls 2019-2020 Thomas Built Saf-T-Liner C2 school buses with optional auxiliary outlets that may shut down engines without restart, risking crashes.
Thomas BuiltDec 21, 2018 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER C2 (2020) recall — Electrical System
Daimler Trucks North America recalls 2019-2020 Thomas Built Saf-T-Liner C2 buses with electrical issues that may cause engine shutdown without restart, increasing crash risk. Owners must contact DTNA for free wiring fix.
Thomas BuiltDec 21, 2018 - Lower riskMedical device
Philips Healthcare recalls DigitalDiagnost C50, Stationary X-ray System
Philips recalls DigitalDiagnost C50 X-ray systems due to a missing label. This may affect safety and compliance. Contact Philips for details.
Philips HealthcareDec 21, 2018 - Lower riskMedical device
Cook Inc. recalls Check-Flo Performer Introducer, Catalog Number RCFW-5.0-25-45-RB-CHB, GPN G11571
Cook recalls Check-Flo Performer Introducer with longer sheaths that may cause injury during use. Affected units include specific catalog and lot numbers. Consumers should contact Cook for details.
CookDec 21, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
Zimmer Biomet recalls Vanguard Knee System Series-A Standard Patella sizes 31mm (Item 184764) due to potential size mismatch with label. Affected patients should contact for details.
Zimmer BiometDec 21, 2018 - Use cautionMedical device
Draeger Medical, Inc. recalls ID Circuit Basic 180, Catalog Number MP01350 Breathing Circuits/Anesthesia Sets without a Water trap: Breathing circuit
Draeger Medical recalls ID Circuit Basic 180 breathing circuits without water traps due to potential short circuits. These single-use anesthesia sets may cause incorrect connections or electrical issues during use.
Draeger MedicalDec 21, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet
Zimmer Biomet recalls specific model of shoulder replacement implants due to potential packaging without taper adapter. Affected units may need verification and action.
Zimmer BiometDec 21, 2018 - Lower riskMedical device
Edwards Lifesciences, LLC recalls Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 131F7P (5 pack of 131F7) Product Usage: The Swan-Ganz
Edwards Lifesciences recalls Swan Ganz Thermodilution Catheters (REF 131F7P) with incorrect lumen assembly that may cause reversed pressure readings. Affected units include specific lot numbers.
Edwards LifesciencesDec 21, 2018 - Use cautionMedical device
Philips Medical Systems Nederlands recalls Achieva XR 1.5T/3.0T, Model Number 781153. Nuclear Magnetic Resonance Imaging System
Philips recalls Achieva XR 1.5T/3.0T MRI systems (model 781153) due to risk of ceiling speakers falling and being pulled by magnetic fields. Affected units must be checked for this hazard.
Philips Medical SystemsDec 21, 2018 - Lower riskDrug
LUPIN SOMERSET recalls Nitrofurantoin Oral Suspension, USP, 25mg/5mL, 230 mL bottle, Rx only, Manufactured by: Novel Laboratories, Inc.,
Lupin Somerset recalls specific lots of Nitrofurantoin Oral Suspension due to subpotent drug levels. This may not provide effective treatment for urinary tract infections. Consumers should check lot numbers and contact the manufacturer for details.
Lupin SomersetDec 21, 2018 - Lower riskFood
US Gypsum recalls Terra Alba Food and Pharmaceutical Grade Hydrous Calcium Sulfate packaged in 50lb paper bags with inner plastic liner.
US Gypsum recalls Terra Al:ba Food Grade Calcium Sulfate in 50lb paper bags with plastic liner due to potential Salmonella contamination. Consumers should check lot numbers for affected products.
US GypsumDec 21, 2018 - Lower riskFood
Pennant Ingredients recalls New & Improved RTU Donut Glaze, NET WEIGHT 2800 lb. (1270 Kg) tote, UPC Codes: 608002213109, Product Code: 4110531
Pennant Ingredients is recalling New & Improved RTU Donut Glaze totes due to potential Salmonella contamination. Consumers should check UPC codes 608002213109 and lot numbers for affected products.
Pennant IngredientsDec 21, 2018 - Lower riskFood
Bornstein Seafoods Inc recalls 5-pound cans of unpasteurized, ready-to-eat, Dungeness crab meat, packaged in reduced oxygen metal cans that were
Bornstein Seafoods recalls 5-pound unpasteurized Dungeness crab meat cans with incorrect temperature indicators that may harbor botulism toxin if temperature abused.
Bornstein SeafoodsDec 21, 2018 - Lower riskFood
Dakota Specialty Milling, Inc recalls Dakota Specialty Milling Milton's MG Premix w Enrichment 94503860, 41820, Net Wt 50 lbs. Yellow Corn, Wheat Bran, Oat
Dakota Specialty Milling recalls Milton's MG Premix w Enrichment 94503860 and 41820 due to potential Salmonella contamination in yellow corn, wheat bran, and oat products.
Dakota Specialty MillingDec 21, 2018 - Lower riskFood
Southwind Foods LLC dba Great American Seafood Imports Co. recalls Wild Dungeness Crab Cake; Net Weight: 12 lb - 48 x 4.0 oz. Keep Frozen Manufactured for Whole Foods Market
Great American Seafood recalls 12-lb Wild Dungeness Crab Cakes sold at Whole Foods Market due to potential temperature abuse. Products were manufactured for Whole Foods Market with lot #18A337-01 and best by 3-2-2019.
Great American SeafoodDec 21, 2018 - Stop using nowFood
Chocolate Therapist, The recalls The Chocolate Therapist, Chocolate Rx, The Purist, 72% Natural Dark Chocolate, Net Wt 2oz (57g)
The Chocolate Therapist recalls select lots of 72% Natural Dark Chocolate because it may contain undeclared milk solids, posing a risk to those with allergies.
The Chocolate TherapistDec 21, 2018 - Use cautionVehicle
HONDA CLARITY FUEL CELL (2018) recall — Electrical System
Honda recalls 2017-2018 Clarify Fuel Cell vehicles with potential power loss causing crashes. Owners must update FC-ECU software for free by Feb 14, 2019.
HondaDec 20, 2018 - Use cautionVehicle
NISSAN ALTIMA (2019) recall — Fuel System, Gasoline
Nissan recalls 2019 Altima vehicles with potential fuel leak risk if retainer clip is unlocked, increasing fire risk. Owners must have fuel hose secured by dealer.
NissanDec 20, 2018 - Use cautionVehicle
JEEP CHEROKEE (2019) recall — Electrical System
Chrysler recalls certain 2019 Jeep Cherokee vehicles due to potential instrument cluster failure causing lack of driver alerts, increasing crash risk. Owners must have instrument clusters inspected or replaced free by dealers.
ChryslerDec 20, 2018 - Use cautionMedical device
Merge Healthcare, Inc. recalls The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product
Merge Healthcare recalls specific models of the Eye Station Retinal Imager (DCF-1024 & DCF-512) due to electrical output exceeding safety limits. This could cause electrical shock during use. Affected units have unique serial numbers listed in the recall notice.
Merge HealthcareDec 20, 2018 - Lower riskMedical device
Terumo Cardiovascular Systems Corporation recalls Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222
Terumo recalls Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) due to natural rubber latex not being declared on label. Affected units have catalog number 140222 and lot numbers V A30.
TerumoDec 20, 2018 - Lower riskMedical device
Becton Dickinson & Co. recalls Phoenix AST Indicator, Catalog Number 246004
Bect: Phoenix AST Indicator (Catalog 246004) with specific batch numbers recalled due to increased test aborts in certain lab panels.
Becton DickinsonDec 20, 2018 - Lower riskMedical device
TERRIFIC CARE LLC recalls CoaguChek XS PT Test; All Catalog/REF Numbers that do NOT end in 160 The CoaguChek XS PT test strips are part of the
Terrific Care recalls CoaguChek XS PT test strips with catalog numbers not ending in 160 due to potential for abnormally high INR results in users who purchased directly from their website or phone.
Terrific CareDec 20, 2018 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls Alinity i Processing Module, (a) Part Number 03R65-01 (b) Part Number A-30108552-01 (c) Part Number A-30109694-01
Abbott recalls Alinity i Processing Modules with specific part numbers due to foaming and dried residue in the buffer reservoir, which may affect test accuracy. Affected units include serial numbers Ai01001-Ai01455, Ai01457, Ai01459.
AbbottDec 20, 2018 - Use cautionMedical device
Steris Corporation recalls AMSCO 5000 Series Washer/Disinfector Model # 5052
Steris recalls AMSCO 5000 Series Washer/Disinfector Model #5052 due to software issues that may cause medical instruments to be inadequately cleaned or disinfected. Affected units have specific serial numbers listed in the recall.
SterisDec 20, 2018 - Lower riskMedical device
GE Healthcare, LLC recalls GE Healthcare Centricity Universal Viewer Breast Imaging Centricity Universal Viewer is a device that displays medical
GE Healthcare recalls Centricity Universal Viewer Breast Imaging versions 6.0 SP4+ with specific workstations due to potential incorrect patient images during image switching, risking misdiagnosis.
GE HealthcareDec 20, 2018 - Lower riskDrug
Amerigen Pharmaceuticals Inc. recalls Temozolomide Capsules, 180 mg, packaged in a 14 count bottles, Rx only, Mfd, by: Stason Pharmaceuticals, Inc., Irvine,
Amerigen Pharmaceuticals recalls 14-count Temozolomide capsules (180mg) due to failed dissolution specifications. Patients should contact their doctor for guidance.
Amerigen PharmaceuticalsDec 20, 2018 - Use cautionDrug
Allergan, PLC. recalls OZURDEX (dexamethasone intravitreal implant) 0.7 mg), 1 single-use plastic applicator contained within carton, Rx only,
Allergan recalls OZURDEX 0.7 mg intravitreal implants (NDC 0023-3348-07) after finding silicone particles during manufacturing. This may cause eye injury. Consumers should contact Allergan for details.
AllerganDec 20, 2018 - UnratedDrug
Akorn Inc recalls COSOPT Ophthalmic Solution, USP, (2% Dorzolamide Hydrochloride, 0.5% Timolol Maleate), 10 mL dropper bottle, Sterile,
Akorn recalls specific lots of COSOPT eye drops distributed nationwide due to failed stability specifications. Check your bottle's lot number and expiration date.
AkornDec 20, 2018 - Stop using nowDrug
Torrent Pharma Inc. recalls LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent
FDA recalls Torrent's 25mg Losartan Potassium Tablets due to NDEA impurity exceeding safe levels. Stop using if you have the specific lot number.
TorrentDec 20, 2018
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