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
35,025 found- Lower riskDrug
KVK-Tech, Inc. recalls Atovaquone Oral Suspension, USP, 750 mg/5 mL, 210 mL bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC
KVK-Tech recalls Atovaquone Oral Suspension (750 mg/5 mL, 210 mL) due to customer reports of unusual grittiness. This medication is prescription-only and may be affected by specific batch numbers.
KVK-TechJul 2, 2021 - Lower riskFood
Caribbean Belize LLC recalls Caribbean Belize Spices Caribbean Rub, Net Wt. 3.5oz (99g) Plastic bottle with black cap Sold as single bottles
Caribbean Belize LLC recalls Caribbean Rub spices due to undeclared wheat allergen. Consumers should check lot numbers and contact the company for details.
Caribbean BelizeJul 2, 2021 - Lower riskFood
Eillien's Candies, Inc. recalls Blain's Farm & Fleet Select Dark Chocolate Amaretto Pecans, 12oz.
Eillien's Candies, Inc. recalls Blain's Farm & Fleet Select Dark Chocolate Amaretto Pecans due to undeclared almonds. Check lot numbers T04 (best by 04/29/22) for affected products.
Blain's Farm & FleetJul 2, 2021 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700
Howmedica Osteonics recalls Triathlon Prim CEM FXD BPLT 7 baseplates with potentially oversized internal profiles that may prevent proper locking of the insert. Affected units include Catalog No. 5520B700, Lot JHS2H.
Howmedica OsteonicsJul 1, 2021 - Lower riskMedical device
Gibson Bioscience recalls Potassium Hydroxide 10% (KOH 10%), Cat. No. 300145 Potassium Hydroxide 10% (KOH 10%) is intended for use in the
Gibson Bioscience recalls KOH 10% solution (Cat. No. 300145) due to hydrogen peroxide contamination. This may cause unintended reactions during lab use. Affected lots include 21137116 with UDI 10634853000633.
Gibson BioscienceJul 1, 2021 - Lower riskMedical device
DePuy Orthopaedics, Inc. recalls ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080
DePuy recalls 16x80mm revision cemented knee stem (part 1512-16-080) due to incorrect size in shipment. Affected units may cause improper fit during surgery.
DePuyJul 1, 2021 - Lower riskMedical device
Beckman Coulter Inc. recalls ACCESS SARS-CoV-2 ANTIGEN QC, REF: C68670, CONTENTS: 3 X 6.0 mL QC1, 3 x 6.0 mL QC2, 1 QC VALUE CARD, IVD, Rx Only,
Beckman Coulter recalls ACCESS SARS-CoV-2 Antigen QC (REF: C68670) due to potential false positive results. This may lead to incorrect COVID-19 diagnoses. Affected units include all lots.
Beckman CoulterJul 1, 2021 - Lower riskMedical device
Verathon, Inc. recalls GlideScope Go Monitors
Verathon recalls GlideScope Go Monitors with specific serial numbers and software versions for potential fluid ingress due to failed IP67 rating, which could cause loss of functionality.
VerathonJul 1, 2021 - Lower riskMedical device
Medline Industries Inc recalls Medline Arthroscopy Kit, convenience kit, REF DYNJ904304B, containing expired component NaCl 3000mL Irrigation Bag
Medline recalls arthroscopy kits with expired NaCl irrigation bags. The expired component poses a risk of ineffective use during surgery. Affected kits contain specific model and expiration dates.
MedlineJul 1, 2021 - Lower riskFood
T & R Enterprises USA, Inc. recalls Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprises St. Louis MO.
T&R Enterprises recalls vegetable egg rolls (96 units 3oz or 120 units 2oz) due to unlabelled Yellow #5 food dye. Best by October 2021.
T&R EnterprisesJul 1, 2021 - Stop using nowConsumer product
TBD Liquids Recalls Liquid Nicotine Products Due to Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
TBD Liquids is recalling liquid nicotine products due to non-child-resistant packaging, which could lead to poisoning if young children access them. Consumers should stop using and store out of reach of children.
TBD LiquidsJul 1, 2021 - Stop using nowConsumer product
Rejuvenation Recalls Deep Frame Mirrors Due to Laceration and Injury Hazards (Recall Alert)
Rejuvenation recalls deep frame mirrors due to glue failure causing detachment and injury risks. Affected models include bronze, brass, and matte white finishes. Consumers should stop using and contact for refund or replacement.
RejuvenationJul 1, 2021 - Use cautionVehicle
PORSCHE CAYENNE (2021) recall — Steering
Porsche recalls certain 2021 Cayenne vehicles due to potential steering column detachment causing loss of control. Owners must contact dealers for free repair by August 24, 2021.
PorscheJun 30, 2021 - Use cautionVehicle
VOLKSWAGEN JETTA (2020) recall — Air Bags
Volkswagen recalls 2020-2021 Jetta models with air bag control module welded incorrectly, risking improper deployment during crashes or unintended activation.
VolkswagenJun 30, 2021 - Lower riskMedical device
CooperSurgical, Inc. recalls Oxygen Sensor Model K54019-2 used in the: G185 & G210 Incubators and G603 Work Chambers Oxygen Sensors supplied for use
CooperSurgical recalls Oxygen Sensor Model K54019-2 used in G185 & G210 Incubators and G603 Work Chambers. Sensors may display incorrect oxygen levels, risking embryo loss during storage.
CooperSurgicalJun 30, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition
GE Healthcare recalls Revolution CT, Revolution CT ES, Revolution Apex, and Revolution CT with Apex edition CT scanners due to potential overdisplay of radiation dose during interventional exams with SmartStep.
GE HealthcareJun 30, 2021 - Use cautionMedical device
Olympus Corporation of the Americas recalls Soltive Premium Super Pulsed Laser System (TFL-PLS) & Pro Super Pulsed Laser System (TFL-SLS). Intended for incision,
Olympus recalls Soltive Premium and Pro Super Pulsed Laser Systems due to risk of thermal injury when treating ureteral stones with settings exceeding 20W. Affected units have Software Version 2.0 and specific serial numbers.
OlympusJun 30, 2021 - Use cautionMedical device
Hitachi Healthcare Americas Corporation recalls Model L43K Intraoperative Probe-For the diagnostic ultrasound evaluation during robotic/non-robotic intra-operative and
Hitachi Healthcare recalls L43K Intraoperative Probes with serial numbers listed; screw cover may fall off after cleaning/sterilization, requiring pre-use checks before procedures.
Hitachi HealthcareJun 30, 2021 - Use cautionMedical device
Aesculap Implant Systems LLC recalls RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Aesculap recalls specific spinal surgery instrument (TEK1940) due to risk of implant deformation during spinal procedures. Affected units sold with lot number 2930902A.
Aescul: Aesculap Implant Systems LLCJun 30, 2021 - Lower riskMedical device
Merit Medical Systems, Inc. recalls Prelude SNAP Splittable Sheath Introducer, REF: PLSX -1010, size 10F, Standard Length: 13 cm, CE0344, STERILE EO, Rx
Merit Medical recalls Prelude SNAP Splittable Sheath Introducer (REF: PLSX-1:10F) due to potential packaging error where 7F sheaths are shipped as 10F. This may cause incorrect use in medical procedures.
Merit Medical SystemsJun 30, 2021 - Lower riskMedical device
BAXTER HEALTHCARE CORPORATION recalls Sharesource Connectivity Platform for Use with the Amia Automated PD System
Baxter Healthcare recalls Sharesource Connectivity Platform for Amia Automated PD Systems due to incorrect UF Limit setting description in user guide, potentially causing therapy errors.
Baxter HealthcareJun 30, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls Revolution Apex, Revolution CT with Apex Edition
GE Healthcare recalls Revolution Apex and Revolution CT with Apex Edition scanners due to potential inaccurate radiation dose displays, which could lead to unnecessary radiation exposure during scans.
GE HealthcareJun 30, 2021 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP
Siemens recalls Artis zee floor, ceiling, and MP models with software version VD12 due to potential startup failures that could delay clinical treatment. Affected units have specific serial numbers listed in the recall notice.
SiemensJun 30, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls The system is intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission
GE Healthcare recalls Revolution CT systems due to potential scan group name input errors causing failed updates. Affected units may not confirm scan group additions, risking incomplete imaging. Contact GE for remedy details.
GE HealthcareJun 30, 2021 - UnratedDrug
Cascade Kelly Holdings LLC recalls Global Hand Sanitizer with moisturizer, Alcohol-based Antiseptic 80%, Non-sterile Topical Solution, 8 fl. oz./236 mL,
Cascade Kelly Holdings recalls alcohol-based hand sanitizer with moisturizer due to CGMP deviations affecting denaturant quality. No remedy specified in official notice.
Cascade Kelly HoldingsJun 30, 2021 - UnratedDrug
Promise Pharmacy, LLC recalls MIC+Methyl B12 injection Methionine Inositol Choline+Methylcobalamin 25 mg/50 mg/50 mg/1 mg/mL, 10 mL vial sterile, Rx
Promise Pharmacy recalls a specific MIC+Methyl B12 injection vial due to lack of processing controls. This medication is prescription-only and may pose risks if not handled properly.
Promise PharmacyJun 30, 2021 - Lower riskFood
Chicken of the Sea; Thai Union recalls Chicken of the Sea Genova Meal Kit; Kits include dry whole wheat pasta, dried basil and parsley, 2 cans of Genova Tuna,
Chicken of the Sea recalls 250 Genova Meal Kits due to quality issues. Kits sold in multiple states may not meet standards.
Chicken of the SeaJun 30, 2021 - Use cautionConsumer product
UPPAbaby Recalls Adapters Included with RumbleSeats Due to Child Fall Hazard
UPPAbaby recalls adapters for RumbleSeat strollers (models 0252, 0917, 0918) from Sept 2014-July 2019 due to fall risk. Affected owners get free replacements if adapters have a yellow tab.
UPPAbabyJun 30, 2021 - Stop using nowConsumer product
Children's Robes Sold Exclusively on Amazon.com Recalled Due to Violation of Federal Flammability Standard and Burn Hazard; Manufactured by SIORO
SIORO recalls children's cotton robes sold on Amazon due to flammability risks. Stop using immediately and contact SIORO for a full refund with free shipping.
SIOROJun 30, 2021 - Stop using nowConsumer product
Children's Nightgowns Sold Exclusively on Amazon.com Recalled Due to Violation of Federal Flammability Standard and Burn Hazard; Manufactured by Booph
Booph's 100% cotton children's nightgowns sold on Amazon fail federal flammability standards, risking burns. Consumers must stop using and return for refund.
BoophJun 30, 2021
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