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[Recalled] White brick oven WHITE BREAD INGREDIENTS: Spring Flour (unbleached), water vegetable shortning... Stahl's Bakery (586) 716-8500 — The finished product labels do not declare sub-ingredients of Wheat (flour) | FDA 2012-04-26

FDA recall notice for White brick oven WHITE BREAD INGREDIENTS: Spring Flour (unbleached), water vegetable shortning... Stahl's Bakery (586) 716-8500 (JDS Baker

[Recalled] Bear Paws MICROWAVEABLE A Pastry Ingredients: Flour (unbleached), powdered sugar, sugar, walnuts, water, vegetable shortening Net Wt 8oz Stahl's Bakery (586) 716-8500 — The finished product labels do not declare sub-ingredients o

FDA recall notice for Bear Paws MICROWAVEABLE A Pastry Ingredients: Flour (unbleached), powdered sugar, sugar, walnuts, water, vegetable shortening Net Wt 8oz S

[Recalled] Cinnamon Rolls A Pastry Ingredients: Spring Flour (unbleached), water, powdered sugar sugar, vegetable shortening Net Wt 8oz Stahl's Bakery (586) 716-8500 — The finished product labels do not declare sub-ingredients of Wheat (flo

FDA recall notice for Cinnamon Rolls A Pastry Ingredients: Spring Flour (unbleached), water, powdered sugar sugar, vegetable shortening Net Wt 8oz Stahl's Baker

[Recalled] The Instructions For Use for the following: Stryker TRIO+ 4.5 x 45 mm STANDARD POST SCREW Stryker TRIO+ 4.5 x 50 mm STANDARD POST SCREW Stryker TRIO+ 4.5 x 55 mm STANDARD POST SCREW Stryker TRIO+ 5.5 x 45 mm STANDARD POST SCR

FDA recall notice for The Instructions For Use for the following: Stryker TRIO+ 4.5 x 45 mm STANDARD POST SCREW Stryker TRIO+ 4.5 x 50 mm STANDARD POST SCREW

[Recalled] The brand name of the device is Damon 3MX Bicuspid Bracket, an orthodontic bracket. Part Number 494-4491, Description -Damon 3MX Bicuspid Bracket, Lot Number - 011265039 Product Usage: Damon 3MX Bicuspid Brackets are inten

FDA recall notice for The brand name of the device is Damon 3MX Bicuspid Bracket, an orthodontic bracket. Part Number 494-4491, Description -Damon 3MX Bicuspid

[Recalled] PUMA USA V-Konstruct Training Jacket with Pockets — This recall involves the USA V-Konstruct Training Jacket with Pockets model num… | CPSC 2012-04-24

CPSC recall notice for PUMA USA V-Konstruct Training Jacket with Pockets. Reason: This recall involves the USA V-Konstruct Training Jacket with Pockets model nu

[Recalled] Lenovo ThinkCentre M70z and M90z computers — The recalled all-in-one desktop computers, or PCs, are flat-panel monitors with… | CPSC 2012-04-24

CPSC recall notice for Lenovo ThinkCentre M70z and M90z computers (Lenovo, of Morrisville, N.C.). Reason: The recalled all-in-one desktop computers, or PCs, are

[Recalled] Me Jane and "B-Hip Kids by Me Jane" girls' jackets with faux fur trim — This recall involves two girls' polyfill jackets with faux-fur trim around the… | CPSC 2012-04-24

CPSC recall notice for Me Jane and "B-Hip Kids by Me Jane" girls' jackets with faux fur trim. Reason: This recall involves two girls' polyfill jackets with faux

[Recalled] Gems 3100 Pressure Detectors/Transducers — The Gems 3100 Pressure Transducer is used to detect pressure in a range of appl… | CPSC 2012-04-24

CPSC recall notice for Gems 3100 Pressure Detectors/Transducers. Reason: The Gems 3100 Pressure Transducer is used to detect pressure in a range of appl…. Issue

[Recalled] Sprouts, Natto Soybean, packed in clear plastic 1.0 lb bags, labeled in part *** Henry's Farm Inc. 5500 Fair Oak Lane, Woodward, VA 22580*** — Soybean sprouts may be contaminated with Listeria monocytogenes | FDA 2012-04-24

FDA recall notice for Sprouts, Natto Soybean, packed in clear plastic 1.0 lb bags, labeled in part *** Henry's Farm Inc. 5500 Fair Oak Lane, Woodward, VA 22580*

[Recalled] LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE; Distributed in the USA by: Stryker Spine. 2 Pearl Ct. Allendale, NJ 07401. Provides access to the thoracic a

FDA recall notice for LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE; Distributed in the U

[Recalled] GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Product Usage: It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images, spectroscopic images, paramet

FDA recall notice for GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Product Usage: It is indicated for use as a diagnostic imaging de

[Recalled] SIGMASpectrum Infusion Pump Master Drug Library (MDL) Editor software. Product Usage: A customized in-house library of all IV and epidural drugs, along with their safe delivery parameters. — Sigma is a safety alert for the

FDA recall notice for SIGMASpectrum Infusion Pump Master Drug Library (MDL) Editor software. Product Usage: A customized in-house library of all IV and ep

[Recalled] Amplilink (AL) Software 3.2.3 for use with COBAS AMPLICOR, CAP/CA, COBAS TaqMan,and COBAS AmpliPrep/COBAS TaqMan. The software can be used with a Laboratory Information System. — When using a Laboratory Information system (LIS) w

FDA recall notice for Amplilink (AL) Software 3.2.3 for use with COBAS AMPLICOR, CAP/CA, COBAS TaqMan,and COBAS AmpliPrep/COBAS TaqMan. The software can be used

[Recalled] Grafton DBM Crunch Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use

FDA recall notice for Grafton DBM Crunch Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with i

[Recalled] Grafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended f

FDA recall notice for Grafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined

[Recalled] Grafton DBM Putty Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use a

FDA recall notice for Grafton DBM Putty Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with in

[Recalled] Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is

FDA recall notice for Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tiss

[Recalled] The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The Centricity Enterprise Web is an image and information distribution system for the clinical

FDA recall notice for The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The

[Recalled] Miflex High Pressure Scuba Diving Hoses — The high pressure hose is used to monitor cylinder pressure for the air supply… | CPSC 2012-04-19

CPSC recall notice for Miflex High Pressure Scuba Diving Hoses (Miflex 2, Villasanta, Italy). Reason: The high pressure hose is used to monitor cylinder pressur