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
RecallCPSC
Toys R Us, Babies R Us And Other Retail Stores Nationwide And On The Internet From September 2008 Through September 2010 For About $4 Per Pair.
The First Years® Recalls American Red Cross® Cabinet Swing Locks; Latches Can Fail to Prevent Access by Children
Toys·41,300 affected·Dec 2, 2010
High RiskFDA
Pride Mobility Products Corp
Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.
Medical Devices·186 affected·Nov 26, 2010
RecallCPSC
Sporting Goods Stores Nationwide Between August 2010 And September 2010 For About $70 Per Half Dozen.
Beman Recalls Bowhunting Arrows; Arrows Can Break and Hit Unintended Targets
Consumer Products·11,300 affected·Nov 16, 2010
CriticalFDA
Physicians Total Care, Inc
Morphine Sulfate Extended Release tablet, 30 mg, 60 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, Ok 74146-6234, NDC 54868-4...
Oral Drugs·540 affected·Nov 10, 2010
CriticalFDA
Physicians Total Care, Inc
Morphine Sulfate Immediate Release tablet, 30 mg/120 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, OK 74146-6234, NDC 5486...
Oral Drugs·600 affected·Nov 10, 2010
High RiskFDA
Canon Inc.
Canon Solid State X-ray Imager (Flat Panel/Digital Imager), Digital Radiography, Models CXDI-55C, CXDI-55G and CXDI-70C. These devices ar...
Diagnostic Devices·468 affected·Nov 1, 2010
RecallCPSC
Automotive Supply, Auto Detailing, Upholstery, Textiles, Furniture And Fabric Stores Nationwide From January 2005 Through August 2010 For About $10.
Claire-Sprayway Recalls Fabric Protector Due to Respiratory Hazard
Consumer Products·73,500 affected·Oct 21, 2010
High RiskFDA
Zimmer, Inc.
00789504001 VerSys Femoral Head Provisional 40mm -3.5 00789504002 VerSys Femoral Head Provisional 40mm +0 00789504003 VerSys Femoral He...
Medical Implants·128,946 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202 MIS 12/14 Slotted Femoral Head Provisional +0X32 00780303203...
Medical Implants·56,516 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780304003...
Medical Implants·56,516 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
00780302201 MIS 12/14 Slotted Femoral Head Provisional -2X22 00780302202 MIS 12/14 Slotted Femoral Head Provisional +0X22 00780302203 M...
Medical Implants·56,516 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
00780303601 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780303602 MIS 12/14 Slotted Femoral Head Provisional +0X36 00780303603...
Medical Implants·56,516 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
. 00789502801 VerSys Femoral Head Provisional 28mm -3.5 00789502802 VerSys Femoral Head Provisional 28mm +0 00789502803 VerSys Femoral ...
Medical Implants·128,946 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
00780302801 MIS 12/14 Slotted Femoral Head Provisional -3.5X28 00780302802 MIS 12/14 Slotted Femoral Head Provisional +0X28 00780302803...
Medical Implants·56,516 affected·Oct 10, 2010
High RiskFDA
Zimmer, Inc.
00780302601 MIS 12/14 Slotted Femoral Head Provisional -3.5X26 00780302602 MIS 12/14 Slotted Femoral Head Provisional +0X26 00780302603...
Medical Implants·56,516 affected·Oct 10, 2010
High RiskFDA
Sunquest Information Systems, Inc.
Sunquest Laboratory LabAccess Results Workstation (LARS)
Medical Devices·151 affected·Oct 5, 2010
High RiskFDA
Medtronic Xomed, Inc.
Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0 Patient Interfaces REF 8253410 (Neuro). LABELING: Box ...
Medical Devices·53 affected·Sep 27, 2010
High RiskFDA
Medtronic Xomed, Inc.
Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0 Patient Interfaces 8253200 (Response) LABELING: Box La...
Medical Devices·464 affected·Sep 27, 2010
High RiskFDA
Medtronic Xomed, Inc.
Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0 Patient Interfaces REF 8253210 (Pulse). LABELING: Box ...
Medical Devices·7 affected·Sep 27, 2010
High RiskFDA
Beckman Coulter Inc.
ISE Electrolyte Reference reagent (for Synchron LX Systems and UniCel DxC 600/800 Systems), Part No. A28937, A28945, 467935, 467915. P...
Diagnostic Devices·718 affected·Sep 22, 2010
High RiskCPSC
Chuck E Cheese's Restaurants From April 2009 Through June 2010 (light-up Rings) And April Through August 2010 (star Glasses).
Chuck E. Cheese’s Recalls Light-up Rings and Star Glasses Due to Ingestion Hazard
Toys·1,100,000 affected·Sep 15, 2010
RecallFDA
Tosoh Bioscience Inc
G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood.
Medical Devices·633 affected·Aug 18, 2010
RecallFDA
Clinical Diagnostic Solutions
Boule Con Diff US Tri Pack, 6 Vials. For in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology...
Diagnostic Devices·532 affected·Aug 4, 2010
RecallFDA
Clinical Diagnostic Solutions
Boule Con-Diff Hematology Control 9 vials. For in vitro diagnostic use as a control to monitor the performance of multi-parameter hema...
Diagnostic Devices·690 affected·Aug 4, 2010
High RiskFDA
Technidata S.a.
TD-Synergy. Laboratory Information System.
Medical Devices·10 affected·Jul 29, 2010
High RiskFDA
Xoran Technologies, Inc.
Xoran Minicat00158
Medical Devices·0 affected·Jul 27, 2010
High RiskFDA
Xoran Technologies, Inc.
Xoran MiniCAT CT Scanner
Medical Devices·320 affected·Jul 27, 2010
High RiskFDA
Xoran Technologies, Inc.
Xoran MiniCAT00202
Medical Devices·320 affected·Jul 27, 2010
High RiskFDA
Kimberly-clark Corporation
Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic gastrostomy (PEG...
Surgical Devices·277 affected·Jun 22, 2010
High RiskFDA
Smiths Medical Asd, Inc.
Medfusion Model 3500 Syringe Pump, Model #3500-415 and 3500-500. Intended for use in critical care areas for the administration of flu...
Medical Devices·6 affected·May 14, 2010
High RiskFDA
Cayenne Medical Inc.
AperFix Femoral Implant Coring Removal Drill, labeled as the following: a. Femoral Removal Coring Reamer 9mm, Model Number CM-7109; ...
Medical Implants·1,444 affected·Apr 28, 2010
RecallCPSC
Specialty Dive Shops Nationwide From July 2008 Through July 2009 For Between $800 And $900 (u.s.) And Between $880 And $990 (canadian).
Dive Computers Recalled by Mares Due to Drowning Hazard
Electronics·600 affected·Apr 14, 2010
RecallCPSC
Authorized Tusa Distributors And Diving And Equipment Stores Nationwide From May 2009 Through September 2009 For About $450.
Tabata USA Recalls Scuba Regulators Due to Drowning Hazard
Consumer Products·250 affected·Apr 13, 2010
CriticalCPSC
Walmart, Burlington Coat Factory, Target, Babies "r" Us, Bj's Wholesale, Various Baby And Children's Stores And Other Retailers Nationwide, And On The Web At Amazon.com January 2003 Through March 2010 For Between $25 And $30.
Infantino Recalls to Replace SlingRider Baby Slings; Three Infant Deaths Reported
Children's Products·1 affected·Mar 24, 2010
High RiskFDA
Physio-control, Inc.
The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor and indoor emergency care settings with...
Cardiac Devices·1,399 affected·Mar 11, 2010
High RiskFDA
K C Pharmaceuticals Inc
Eye Drops advanced relief (Dextran 70 0.1%, Polyethylene glycol 400 1%, Povidone 1%, Tetrahydrozoline HCl 0.05%) ophthalmic solution, 1/2...
Ophthalmic Drugs·31,704 affected·Mar 1, 2010
High RiskFDA
Lockheed Martin Gyrocam Systems, Inc.
Lockheed Martin Gyrocam Systems ( LMGS) LMGS 15" camera systems. Laser pointer and illuminator used for law enforcement surveillance from...
Medical Devices·33 affected·Jan 21, 2010
Medium RiskCPSC
Babies "r" Us, Kmart, Sears, Target And Walmart From January 2007 Through October 2009 For Between $100 And $130.
Dorel Juvenile Group Recalls Play Yards with Bassinets Due to Suffocation Hazard
Children's Products·213,000 affected·Dec 30, 2009
RecallCPSC
Authorized Dive Shops Nationwide And On The Internet From March 2009 Through August 2009 For Between $280 And $309.
Scuba Regulators Recalled by Cressi Due to Risk of Drowning
Consumer Products·200 affected·Dec 23, 2009
RecallCPSC
Diving Equipment Retailers And Distributors Nationwide From June 2006 Through October 2008 For About $359.
Diving Equipment Recalled by Dive Rite Due to Drowning Hazard
Consumer Products·16,000 affected·Dec 22, 2009
RecallCPSC
Home Depot, Lowe's, Menards, Sears, Walmart, Hardware Stores And By Independent Dealers From November 2008 Through October 2009 For Between $1,000 And $2,300.
MTD Recalls Log Splitters Due to Amputation Hazard
Consumer Products·26,000 affected·Dec 10, 2009
High RiskFDA
Gmp Laboratories Of America Inc
Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDI...
Baby Food & Formula·1,027 affected·Dec 8, 2009
High RiskFDA
Carefusion Corporation
Pyxis Anesthesia System Model 2000 (PAS 2000) Product Usage: The PAS 2000 is an anesthesia medication dispensing device that provid...
Medical Devices·2,637 affected·Nov 20, 2009
High RiskFDA
Terumo Cardiovascular Systems Corporation
Terumo Backplate Replacement CXFVR 1500 Holder The Flexible venous Reservoir is mounted on the Backplate/Holder and secures the flexib...
Medical Devices·33 affected·Oct 2, 2009
RecallCPSC
Diving Equipment Retailers And Distributors From January 2006 Through December 2008 For Between $350 And $450 For The Buoyancy Compensator Devices (bcds) And Between $50 And $275 For The Inflatable Devices.
Diving Equipment Recalled by Halcyon Manufacturing Due to Drowning Hazard
Consumer Products·20,300 affected·Oct 1, 2009
High RiskFDA
Terumo Cardiovascular Systems Corporation
Safety monitor included with System 8000 Base The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the e...
Medical Devices·8 affected·Aug 12, 2009
High RiskFDA
Baxter Healthcare Corp.
Baxter's elastomeric infusion pumps are non-electronic, ambulatory, disposable devices that deliver continuous medication for periods of ...
Medical Devices·2 affected·Jul 31, 2009
High RiskFDA
Baxter Healthcare Corp.
Baxter's elastomeric infusion pumps are non-electronic, ambulatory, disposable devices that deliver continuous medication for periods of ...
Medical Devices·2 affected·Jul 31, 2009