Hazard Type
Other Recalls
21,986 product recalls involving other. Search official CPSC, FDA, and USDA datasets for every recall issued due to this hazard.
21,986Total Recalls
1,733Critical
7708.6MUnits Affected
All Recalls
Every Other Recall
Sorted by most recent. Click any recall for full details and safety information.
21,986 recalls
High RiskFDA
Teleflex Medical
Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Aquapak 640 SW, 650 mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Aquapak 101 SW, 190, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Argon Medical Devices, Inc
UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 32402540 (40 cm) ...
Surgical Devices3,783 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Aquapak 640 SW, 650 mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Adaptor, 040 Hum, International, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Humidifier Adaptor 040, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Aqua 540 SW, 540 w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Aquapak 340 SW, 340, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Teleflex Medical
Aquapak 340 SW, 340, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.
Respiratory Devices7,758,650 affectedJun 5, 2014
High RiskFDA
Nellcor Puritan Bennett Inc. (dba Covidien Lp)
Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a component of the Puritan Bennett 840 Ventilator: The Backlight Inv...
Respiratory Devices7,371 affectedJun 4, 2014
High RiskFDA
Deroyal Industries Inc
DeRoyal KNEE ARTHROSCOPY PACK, REF 89-6192.04, 1 Per Pack, Distributed by: DeRoyal Industries, Inc.; Manufacturer: DeRoyal Industries,...
Medical Devices128 affectedJun 4, 2014
CriticalFDA
Rite Aid Hdqtrs. Corp.
waxed paperboard int container of frozen ice cream labeled Thrifty Ice Cream Mint 'N' Chip 1 Pint (16 Fl. OZ.) Bottom of containe...
Dairy560 affectedJun 3, 2014
High RiskFDA
Instrumentation Laboratory Co.
ACL TOP 500 CTS, automated coagulation laboratory instrument.
Medical Devices2,802 affectedJun 3, 2014
High RiskFDA
Depuy Orthopaedics, Inc.
RECLAIM DISTAL TAPERED, Angled Distal Stem, various sizes. Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgica...
Surgical Devices10,467 affectedJun 3, 2014
High RiskFDA
Instrumentation Laboratory Co.
ACL TOP (Base), automated coagulation laboratory instrument.
Medical Devices1,074 affectedJun 3, 2014
High RiskFDA
Instrumentation Laboratory Co.
ACL TOP 700, automated coagulation laboratory instrument.
Medical Devices633 affectedJun 3, 2014
High RiskFDA
Nellcor Puritan Bennett Inc. (dba Covidien Lp)
Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or non-invasive ventilato...
Respiratory Devices104 affectedJun 3, 2014
High RiskFDA
Instrumentation Laboratory Co.
ACL TOP 700 LAS, automated coagulation laboratory instrument.
Medical Devices99 affectedJun 3, 2014
High RiskFDA
Instrumentation Laboratory Co.
ACL TOP 700 CTS, automated coagulation laboratory instrument.
Medical Devices266 affectedJun 3, 2014
High RiskFDA
Depuy Orthopaedics, Inc.
RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the locking taper surf...
Surgical Devices814 affectedJun 3, 2014
High RiskFDA
Maui Soda & Ice Works Ltd/dba Roselani Ice Cream
Roselani Tropics Kona Mud Mud Pie Ice Cream: 1.75QT, - 56 oz. carton. Maui Soda & Ice Works, Ltd. Wailuku, HI
Dairy2,045 affectedJun 2, 2014
High RiskFDA
Frito-lay, Inc
Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package, UPC 2840007189
Food1,757,772 affectedJun 2, 2014
High RiskFDA
Unit Dose Solutions Inc
Atorvastatin Calcium 40 MG Tablet, MFG: Apotex NDC# 6050525808
Oral Drugs1,177 affectedJun 2, 2014
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus instrument access door hinge. Siemens Healthcare Diagnostics, Inc...
Diagnostic Devices40 affectedJun 2, 2014
High RiskFDA
Siemens Healthcare Diagnostics, Inc
ADVIA Centaur¿ Systems TnI-Ultra assay; Catalog Number 02789602 (100 tests), SMN 10317708 and 02790309 (500 tests), SMN 10317790
Diagnostic Devices34,283 affectedMay 30, 2014
High RiskFDA
Carestream Health Inc.
KODAK DirectView DR 9000 System, Catalog Numbers 1966688 (US and Canada) and 8161937 (outside the US and Canada) --- A permanently inst...
Diagnostic Devices100 affectedMay 30, 2014
High RiskFDA
Teva Pharmaceuticals Usa
Fluvastatin Capsules USP, 20 mg, Rx Only, 30-count bottle, manufactured for Teva Pharmaceuticals, Sellersville, PA, by Teva Pharmaceutica...
Oral Drugs8,472 affectedMay 29, 2014
High RiskFDA
B. Braun Medical, Inc.
STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches
Medical Devices10,835 affectedMay 29, 2014
High RiskFDA
Mckesson Medical Immaging
Horizon Medical Imaging Horizon Medical Imaging is a medical image and information management application that is intended to receive ...
Medical Devices659 affectedMay 29, 2014
High RiskFDA
Kerr Corporation
Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294. The intended use of this device is to be used as a...
Medical Devices2,030 affectedMay 29, 2014
CriticalFDA
Nitinol Devices And Components, Inc.
HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180 CM Length; Manufactured for Covidien, Plymouth, MN; Man...
Surgical Devices8,485 affectedMay 28, 2014
High RiskFDA
Dot Foods Inc.
Large Pitted Kalamata Olives, packaged in 4.4lb black plastic barrels. Labeling reads in part: Savor Greek Large Pitted Kalamata Olives, ...
Food720 affectedMay 27, 2014
High RiskFDA
Dr. Reddy's Laboratories, Inc.
Dr. Reddy's Metoprolol Succinate Extended Release Tablets, USP 25 mg. 100-count bottle, Rx only, Manufactured By: Dr. Reddy's Laboratori...
Oral Drugs13,560 affectedMay 23, 2014
High RiskFDA
Elekta, Inc.
MOSAIQ, an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among h...
Medical Devices723 affectedMay 23, 2014
High RiskFDA
Siemens Healthcare Diagnostics Inc
RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500 Measurement Cartridge Lactate (750 Tests) Part number: 10491449; R...
Medical Devices20,507 affectedMay 23, 2014
High RiskFDA
Aidarex Pharmaceuticals Llc
Ciprofloxacin 500 mg tablets, 20 count bottle, Rx only, Packaged by Aidarex Pharmacecuticals LLC, MFG: Unique Pharmaceutical Laboratories...
Oral Drugs531 affectedMay 22, 2014
High RiskFDA
Sandoz, Inc
Cefpodoxime Proxetil Tablets, USP, 200 mg, 20 Tablet Bottles, Rx Only. Manufactured in Austria by Sandoz GmbH for Sandoz Inc. Princeton, ...
Oral Drugs22,818 affectedMay 22, 2014
Medium RiskFDA
Valeant Pharmaceuticals North America Llc
Vaseretic (enalapril maleate/hydrochlorothiazide) 10/25 mg Tablets, NDC 0187-0146-01, 100 ct. bottles manufactured at Valeant Pharmaceut...
Oral Drugs205,853 affectedMay 21, 2014
Medium RiskFDA
Valeant Pharmaceuticals North America Llc
Vasotec (enalapril maleate) tablets, RX only, Manufactured by Valeant Pharmaceuticals International, Inc., Steinbach, MD R5G 1Z7 Canada ...
Oral Drugs205,853 affectedMay 21, 2014
High RiskFDA
Intuitive Surgical, Inc.
IRK QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System and Si-e. Intuitive Surgical Endoscopic ...
Surgical Devices2,014 affectedMay 21, 2014
RecallFDA
Becton Dickinson & Co.
BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System, catalog number 245000. in vitro diagnostic for the identificatio...
Diabetes Devices18 affectedMay 21, 2014
High RiskFDA
Intuitive Surgical, Inc.
System Manual for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic Instr...
Surgical Devices2,014 affectedMay 21, 2014
High RiskFDA
Intuitive Surgical, Inc.
Connection QRG for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System . Intuitive Surgical Endoscopic I...
Surgical Devices2,014 affectedMay 21, 2014
High RiskFDA
Seaspine Inc
Integra UCR 3mm Hex, Large Axial Driver. The UCR Hex Axial Driver is a surgical instrument used to implant and remove polyaxial screws...
Medical Implants7 affectedMay 21, 2014
High RiskFDA
Intuitive Surgical, Inc.
Stapler Addendum for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic ...
Surgical Devices2,014 affectedMay 21, 2014
High RiskFDA
Intuitive Surgical, Inc.
Insert for IRK for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical Endoscopic In...
Surgical Devices2,014 affectedMay 21, 2014
High RiskFDA
Intuitive Surgical, Inc.
Vision Troubleshooting Guide for the da Vinci Standard Surgical System; da Vinci S System and da Vinci Si System. Intuitive Surgical...
Surgical Devices2,014 affectedMay 21, 2014