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
34,896 found- Lower riskDrug
Milbar Laboratories, Inc. recalls T Shampoo For Hair and Body, Solution Coal Tar 3% (0.6% coal tar), 300 ml/10.1 fl. oz. bottles, Dermatologic Cosmetic
Milbar recalls coal tar shampoo bottles with subpotent coal tar content. This may not deliver intended treatment for skin conditions. Consumers should check lot numbers and expiration dates.
MilbarMay 4, 2018 - Lower riskFood
The C.F. Sauer Company recalls Code - Red Pepper Seasoning (21 oz.) Net Weight: 21 oz., Number of Units per Package: 6 Package Type: clear, 32 fl. oz.
C.F. Sauer recalls 21 oz. red pepper seasoning with undeclared milk allergen. Consumers should check lot codes for affected products to avoid allergic reactions.
C.F. SauerMay 4, 2018 - Lower riskMedical device
Medtronic Neurosurgery recalls Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5
Medtronic recalls Clip Gun Magazines with potentially undetected packaging seal breaches that could compromise sterility during surgery. Affected units have specific lot numbers and are sold in sealed pouches.
MedtronicMay 3, 2018 - Use cautionMedical device
Joerns Healthcare recalls P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS, NYLON, MATERIAL NUMBER PMP3676NZBA (b) PROMATT PLUS 84" MATRESS, NYLON,
Joerns Healthcare recalls specific P.R.O. Matt mattresses with missing internal shutoff valves that could allow air to escape, risking improper therapy use. Affected models include PROMATT PLUS 36x76 and 84" mattresses with listed serial numbers.
Joerns HealthcareMay 3, 2018 - Use cautionMedical device
Philips Electronics North America Corporation recalls HeartStart MRx Monitor/Defibrillator, Model No. M3535A (861288), M3536A (861289) Product Automated external
Philips recalls HeartStart MRx defibrillators (models M3535A and M3536A) due to potential charging failure that could interrupt therapy. Affected units sold in the US from 2018-2020.
PhilipsMay 3, 2018 - Use cautionMedical device
Maquet Datascope Corp - Cardiac Assist Division recalls CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding
Maquet recalls Cardiosave Hybrid Intra-Aortic Balloon Pumps with specific part numbers and serial dates due to fluid ingress risk affecting therapy.
MaquetMay 3, 2018 - Use cautionMedical device
Ethicon Endo-Surgery Inc recalls HARMONIC ACE Shears + Adaptive Tissue Technology, 5mm Diameter / 36cm Length / Curved, Product Code HAR36, GTIN
Ethicon recalls HARMONIC ACE Shears with possible internal component causing unintended activation. Affected models include specific product codes and GTINs. Consumers should contact Ethicon for details.
EthiconMay 3, 2018 - Use cautionMeat & poultry
JBS USA, Inc. Recalls Ground Beef Products Due to Possible Foreign Matter Contamination
JBS USA recalls ground beef products from March 2018 that may contain hard plastic. Consumers are urged not to eat these items and should discard or return them to the store.
JBSMay 2, 2018 - Use cautionVehicle
FREIGHTLINER M2 (2017) recall — Equipment
Ferrara recalls 2017 Freightliner M2 fire trucks with Hale pressure relief valves that may corrode, reducing water pressure during fires. Owners must replace the retaining ring with stainless steel.
FerraraMay 2, 2018 - UnratedMedical device
Smith & Nephew, Inc. recalls smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM, 12/14 TAPER, 7H SIZE, 32 MM x 112 MM, REF 71356107 Hip prosthesis.
Smith & Nephew recalls hip prostheses with undersized taper length that could cause improper fit during surgery. Affected models include Anthology Porous High Offset Stem, 7H size, 32mm x 112mm, lot numbers 17LM22019, 17LM10934, 17LM05900.
Smith & NephewMay 2, 2018 - Lower riskMedical device
Heartware recalls Heartware Medtronic HVAD System for cardiac use. Including the following parts: (a) Controller / Controller Kits,
Heartware Medtronic HVAD System for cardiac patients with controller kits and adapters may experience brief electrical interruptions causing beeping. Affected units have specific product numbers and serials. Contact Heartware for details.
HeartwareMay 2, 2018 - Stop using nowMedical device
Ad-Tech Medical Instrument Corporation recalls AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the
Ad-Tech Medical recalls drill sleeve guides DSG-6.3-090-2.4N with specific batch numbers due to potential drill bit seizing during skull surgery. Affected units may cause serious injury.
Ad-Tech MedicalMay 2, 2018 - Lower riskMedical device
Roche Molecular Systems, Inc. recalls MagNA Pure 24 System, GMMI: 07290519001 Product Usage: The MagNA Pure 24 System is a fully automated clinical sample
Roche recalls MagNA Pure 24 System due to reported cross-contamination of samples during rack-based purification runs. Affected units have specific model numbers and were sold for clinical use.
RocheMay 2, 2018 - UnratedMedical device
Stryker Neurovascular recalls AXS Infinity LS Long Sheath:((6F/.088in)/ x 70cm GEN-10800-70, (6F/.088in)/ x 80cm GEN-10800-80, (6F/.088in)/ x 90cm
Stryker recalls specific AXS Infinity LS Long Sheath models due to outer diameter specification being exceeded. Affected units include GEN-10800-70, GEN-10800-80, and GEN-10800-90 models. No remedy is stated in the recall notice.
StrykerMay 2, 2018 - Stop using nowMedical device
The Seaberg Company Inc recalls Part #: SAM XT-M, Model: Tactical Black or Military
Seaberg recalls Tactical Black or Military belts (SAM XT-M) due to potential buckle failure that could stop blood flow, risking serious injury or death. Affected units include specific lot numbers.
SeabergMay 2, 2018 - Lower riskMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This
Fresenius Medical Care recalls NaturaLyte Liquid Acid Concentrate for Bicarbonate Dialysis due to mislabeled part numbers. This affects 3.43L bottles with part number 08-3231-1. No action is required as the product is safe but must be correctly labeled.
Fresen:iusMay 2, 2018 - Use cautionMedical device
Galt Medical Corporation recalls 1) Drainer Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-001-05, b) DRC-001-06, c) DRC-001-15, 2) Centeze
Galt Medical recalls specific Drainer Centesis Catheters (catalog numbers DRC-001-05 to DRC-001-15 and DRC-002-02 to DRC-002-08) due to potential unsafe bacterial endotoxin levels that could cause fever, chills, and low blood pressure.
Galt MedicalMay 2, 2018 - Stop using nowFood
National Foodworks Services recalls Soozie s Doozies Sugar Cinnamon Snickerdoodle Cookie Dough, 16 ounce, plastic pouch, 6 pouches per case
National Foodworks Services recalls Soozie's Doozies Sugar Cinnamon Snickerdoodle Cookie Dough due to Staphylococcus aureus contamination. Check your lot numbers.
Soozie's DooziesMay 2, 2018 - Stop using nowFood
Flowers Bakery Of Montgomery LLC recalls Hot Dog Buns
Flowers Bakery of Montgomery LLC recalls Hot Dog Buns due to undeclared milk and soy allergens. Check lot numbers A108492, A108449, C108492.
Flowers BakeryMay 2, 2018 - Stop using nowFood
Utz Quality Food Inc recalls Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16
Utz Quality Foods recalls select white corn tortilla chips with Jun 16 2018 expiration dates due to potential undeclared milk allergen contamination.
UtzMay 2, 2018 - Lower riskFood
Badger Botanicals LLC recalls Acadica Kratom: Green Suma, 250g bags
Badger Botanicals recalls Green Suma Kr: 250g bags made between Jan 2018 and Apr 2018 due to potential salmonella contamination. Consumers should check product dates and contact for details.
Badger BotanicalsMay 2, 2018 - Stop using nowConsumer product
Carter's Recalls Children's Cardigan Sets Due to Choking Hazard
Carter's recalls 3-piece penguin cardigan sets for young children due to choking hazard from detachable toggle buttons. Affected sets sold in newborn to 24 months sizes with specific style numbers and UPCs.
Carter'sMay 2, 2018 - Stop using nowVehicle
MCLAREN MP4-12C (2013) recall — Air Bags
McLaren is recalling 2013 MP4-12C vehicles with faulty air bag inflators that may explode during crashes, risking serious injury or death. Owners must have the front passenger air bag inflator replaced free of charge.
McLarenMay 1, 2018 - Stop using nowMedical device
Philips Medical Systems Nederlands recalls OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
Philips Medical Systems recalls specific OmniDiagnost-Eleva X-ray systems due to risk of table rotation causing patient falls. Affected units have product numbers listed in the recall notice.
Philips Medical SystemsMay 1, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000
Siemens recalls ARTIS Pheno Interventional Fluoroscopic X-Ray System Model 10849000 due to potential patient injury from C-arm drop when manually extended.
SiemensMay 1, 2018 - Lower riskMedical device
Hobbs Medical, Inc. recalls Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained
Hobbs Medical recalls bronchial cytology brushes (models 4202, 4204, 4206) that were marketed for uses outside FDA clearance. These brushes are intended for trained medical professionals during endoscopic procedures.
Hobbs MedicalMay 1, 2018 - Lower riskMedical device
Keystone Dental Inc recalls Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or
Keystone Dental recalls Prima Plus implants (Catalog 15737K) due to mislabeling. Affected implants may not be correctly identified for dental use. Consumers should contact Keystone Dental for details.
Keystone DentalMay 1, 2018 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Artis Q.zen floor, Material no. 10848353, for angiography and whole body radiographic/fluoroscopic procedures.
Siemens recalls Artis Q.zen floor model 10848353 for angiography procedures due to display issues after power save mode. The system may not show images and require treatment cancellation.
SiemensMay 1, 2018 - Lower riskMedical device
TP Orthodontics, Inc. recalls Jasper Vektor, Class II Correction Appliance, Part No. 610-527R used for correcting class 2 malocclusions by applying
TP Orthodontics recalls Jasper Vek: Class II Correction Appliance Part No. 610-527R due to 106 complaints of breaking in patients' mouths, risking injury.
TP OrthodonticsMay 1, 2018 - Use cautionDrug
AuroMedics Pharma LLC recalls Piperacillin and Tazobactam for Injection, USP 3.375 grams per vial, For Intravenous Use Only, Single-Dose vial, Rx
AuroMedics Pharma recalls single-dose vials of Piperac:illin-Tazobactam injection due to confirmed visible particulate matter (glass) in some units. This may cause serious injury during IV administration. Affected units have specific NDC and lot numbers.
AuroMedicsMay 1, 2018
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