Recall archive
31,892 recalls · page 408 of 1329
Reported Jul 27, 2022
(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
SX-One MicroKnife
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonex Health LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 27, 2022
YelloPort Elite Universal Seal. For use in laparoscopic procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgical Innovations Ltd.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Synapse Biomedical Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
9-inch pie Blazos Pie Shoppe Chocolate Peanut Butter Cream Pie (UPC 9438600049) 9-inch pie Blazos Pie Shoppe Peanut…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tarts A La Carte, LLC dba Blazo Pie shoppe LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2022
Hydrogen Peroxide Topical Solution USP, 3%, 16 FL OZ (1 PT) 473 mL bottle, packaged as a) Signature Care NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vi-Jon, LLC
FDA (openFDA drug enforcement)
Reported Jul 27, 2022
X80 RADiant Photoelectric Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xstrahl Limited
FDA (openFDA device enforcement)
Consumer productsReported Jul 21, 2022
Aqualung Recalls i330R SCUBA Diving Computers Due to Injury and Drowning Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aqua Lung
CPSC
Consumer productsReported Jul 21, 2022
Vichy Laboratoires Recalls LiftActiv Peptide-C Ampoules Due to Laceration Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cosmetique Active Internationale
CPSC
Consumer productsReported Jul 21, 2022
Crye Precision Recalls LRB™ Leg Loops Due to Fall Hazard (Recall Alert)
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Crye Precision LLC
CPSC
Consumer productsReported Jul 21, 2022
The Hammock Source Recalls Key West Knock Down Hammock Stands Due to Fall Hazard; Sold Exclusively at Lowe's
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hatteras Hammocks, Inc. dba The Hammock Source
CPSC
Consumer productsReported Jul 21, 2022
Silicone Baby Toy Bear Activity Toys Recalled Due to Laceration Hazard; Manufactured by Konges Sløjd Denmark A/S
High riskUsing this product could cause serious injury, illness or death — stop using it now.Konges Sløjd A/S
CPSC
Consumer productsReported Jul 21, 2022
Monti Kids Recalls Toy Box with Bins Due to Choking Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Monti Kids Inc.
CPSC
Reported Jul 20, 2022
AESCULAP TC COOELY MICRO NEEDLEHLDER SERR 200MM, product code MG524R. manual surgical instrument designed to grasp a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Agilent Technologies, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Alcon Custom Pak Surgical Procedure Pack: 16998-11 2519351H SALAHUDDIN 2.4 PACK FRESNO SURGICAL HOSP 18392-03 14HDFF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research, LLC
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Natreve Vegan Protein Powder 10 servings, 13.1oz (371g), UPC 628831120003 18 servings, 1.47lbs/23.53oz (667g), UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arborypharm Foods Inc.
FDA (openFDA food enforcement)
Reported Jul 20, 2022
1st Phorm High Quality Protein Level-1 Bar Chocolate Crunch Protein Bars. 15 Bars Per Box. Net Wt. 12-2.22oz (63g) Bars…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bakery Barn, LLC
FDA (openFDA food enforcement)
Reported Jul 20, 2022
Vivo 45LS Ventilator- intended to provide continuous or intermittent ventilatory support for the care of individuals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breas Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Morphine Sulfate extended-Release Tablets, USP; 30 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bryant Ranch Prepack, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 20, 2022
Pressure Monitoring Set, Single-lumen uncoated central venous catheter. RPN C-PMS-250, GPN G02838
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Incorporated
FDA (openFDA device enforcement)
Reported Jul 20, 2022
PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
RecallNow is not a government agency. Every notice above is published by the FDA, USDA FSIS, or CPSC and links back to its source. Back to the look-up