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All Product Recalls

78,569 recalls

Source:AllCPSCFDAUSDASeverity:AllCriticalHighMedium
High RiskFDA
Acclarent, Inc.
Inspira AIR Balloon Dilation system. Size 5 x 24 mm, Syringe volume 6-8 cc. Dilation of airway tree.
Medical Devices·1,920 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx90 GUIDING CATH MCV Product Code: GCB50900000 Intended for use in the coronary, peripheral, and neurovasculature for int...
Diagnostic Devices·5 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx90 GUIDING CATH MPC Product Code: GMC50900000 Intended for use in the coronary, peripheral, and neurovasculature for int...
Diagnostic Devices·202 affected·Jan 11, 2013
High RiskFDA
Acclarent, Inc.
Inspira AIR Balloon Dilation system. Size 10 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
Medical Devices·2,703 affected·Jan 11, 2013
High RiskFDA
Synthes Usa Hq, Inc.
Synthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Core 40 mm Thread Length, Part Number 487.072. Intended to provide precise a...
Medical Devices·18 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx100 GUIDING CATH ST Product Code: GST51000000 Intended for use in the coronary, peripheral, and neurovasculature for int...
Diagnostic Devices·46 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000 Intended for use in the coronary, peripheral, and neurovasculature for intr...
Diagnostic Devices·19 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 6Fx100 GUIDING CATH HH Product Code: GHH61000000 Intended for use in the coronary, peripheral, and neurovasculature for int...
Diagnostic Devices·25 affected·Jan 11, 2013
High RiskFDA
Synthes Usa Hq, Inc.
Synthes Multi-Vector Distractor - Multi-axial Mandible Distractor (Left), Part Number 487.967. For mandibular bone lengthening.
Medical Devices·18 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx90 GUIDING CATH HH Product Code: GHH50900000 Intended for use in the coronary, peripheral, and neurovasculature for intr...
Diagnostic Devices·141 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for use in the coronary, peripheral, and neurovasculature for int...
Diagnostic Devices·32 affected·Jan 11, 2013
High RiskFDA
Acclarent, Inc.
Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm, Syringe volume 12 cc. Dilation of airway tree.
Medical Devices·625 affected·Jan 11, 2013
High RiskFDA
Acclarent, Inc.
Inspira AIR Balloon Dilation system. Size 12 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
Medical Devices·1,217 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for use in the coronary, peripheral, and neurovasculature for int...
Diagnostic Devices·867 affected·Jan 11, 2013
High RiskFDA
Synthes Usa Hq, Inc.
Variable Angle Locking Compression Plate/VA-LCP Dorsal Distal Radius Plate, Part Number 02.115.431. Indicated for: Dorsally displaced ...
Medical Devices·4 affected·Jan 11, 2013
High RiskFDA
Synthes Usa Hq, Inc.
Synthes Multi-Vector Distractor Body, Part Number 487.931. For mandibular bone lengthening.
Medical Devices·2 affected·Jan 11, 2013
High RiskFDA
Codman & Shurtleff, Inc.
NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for use in the coronary, peripheral, and neurovasculature for intr...
Diagnostic Devices·46 affected·Jan 11, 2013
High RiskFDA
Acclarent, Inc.
Inspira AIR Balloon Dilation system. Size 14 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.
Medical Devices·3,324 affected·Jan 11, 2013
High RiskFDA
Synthes Usa Hq, Inc.
Flexible Grip which is part of the Synthes Universal Nail System. Indicated for the conventional (non-locking) technique of treating s...
Medical Devices·328 affected·Jan 11, 2013
RecallCPSC
Can-am Dealers Nationwide From April 2011 Through December 2012 For Between $11,700 And $21,000.
BRP Recalls Can-Am Side-By-Side Vehicles Due to Loss of Steering Control Hazard
Vehicles / Atvs·3,400 affected·Jan 10, 2013
RecallCPSC
Scuba Diving Retailers Nationwide From April 2012 Through June 2012 For About $34.
High-Pressure Scuba Diving Air Hoses Recalled by A-Plus Marine Due to Drowning Hazard
Consumer Products·40 affected·Jan 10, 2013
CriticalCPSC
John Deere Dealers Nationwide From August 2012 Through October 2012 For Between $12,900 And $15,500.
John Deere Recalls Gator Utility Vehicles Due to Fire Hazard
Vehicles / Atvs·4,650 affected·Jan 10, 2013
RecallFDA
Jmt Trading Company, Inc.
Tausi Salted Black Beans, 180 gram (6.34 oz.) can. Ingredient: Black Beans, Water, Iodized salt, sugar and caramel. Distributed by V8 C...
Beverages·150 affected·Jan 10, 2013
High RiskFDA
Hospira, Inc.
Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04
Injectable Drugs·63,900 affected·Jan 10, 2013
High RiskFDA
Extremity Medical Llc
Extremity Medical - Disposable Orthopedic Surgical Instrument - 1.6 mm Guidewire - Reference Number 101-00006 - Non-Sterile. Contained i...
Surgical Devices·238 affected·Jan 10, 2013
CriticalCPSC
The Recalled Battery Packs Were Sold With Columbia Electric Jackets Sold By Columbia Online And At Columbia Sportswear Stores In The Cities And States Listed Below Between September And November 2012 For About $260. The Nine Columbia Sportswear Outlets That Carried The Jackets With Battery Packs Are Located In: Sunrise, Fla. 33304 Wrentham, Mass. 02093 Birch Run, Mich. 48415-9496 Albertville, Minn. 55301 Central Valley, N.y. 10917 Las Vegas, Nev. 89106 Grove City, Penn. 16127 Park City, Utah 84098 Pleasant Prairie, Wis. 53158-1705
Columbia Sportswear Reannounces Its Recall of Batteries Sold With Jackets Due To Fire Hazard
Electronics·66 affected·Jan 9, 2013
RecallCPSC
Polaris Dealers Nationwide From July 2012 Through September 2012 For About $8,300.
Polaris Recalls Ranger Recreational Off-Highway Vehicles Due to Loss of Control and Crash Hazard
Vehicles / Atvs·327 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of pineapple flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of blueberry flavored powder and sold under the Boba Direct, Inc. brand.
Produce·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of mango flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of vanilla flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of avocado flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of cherry flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of chocolate flavored powder and sold under the Boba Direct, Inc. brand.
Snacks & Candy·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of lychee flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of coconut flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of almond flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of strawberry flavored powder and sold under the Boba Direct, Inc. brand.
Produce·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of cafe latte flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of banana flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of red bean flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of passion fruit flavored powder and sold under the Boba Direct, Inc. brand.
Produce·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of watermelon flavored powder and sold under the Boba Direct, Inc. brand.
Beverages·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of peppermint flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Penzeys Ltd
Vietnamese Cinnamon Extra Fancy, product code 43200, Penzeys Spices, Wauwatosa, WI 53222. to be completed
Food·47 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of lavender flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of taro flavored powder and sold under the Boba Direct, Inc. brand.
Food·0 affected·Jan 9, 2013
High RiskFDA
Boba Direct, Inc.
Foil bags containing 2.2 lbs. each of green tea flavored powder and sold under the Boba Direct, Inc. brand.
Beverages·0 affected·Jan 9, 2013