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[Recalled] KIT,DISPOSABLE ACCESSORY,4ARM,IS2000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vi

FDA recall notice for KIT,DISPOSABLE ACCESSORY,4ARM,IS2000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment fr

[Recalled] AUTOMIX High Speed Compounder System, product 2M8077; automated nutrition compounders; Product Usage: The Automix Compounder Systems are electromechanical positive displacement fluid compounding devices used in the admixture

FDA recall notice for AUTOMIX High Speed Compounder System, product 2M8077; automated nutrition compounders; Product Usage: The Automix Compounder Systems

[Recalled] KIT,DISPOSABLE ACCESSORY,3ARM,IS3000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vi

FDA recall notice for KIT,DISPOSABLE ACCESSORY,3ARM,IS3000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment fr

[Recalled] Strawberry Filled Cake, 21.9 oz (1lb 6oz) (620g), UPC 3 760147 195867 — The recall was initiated because Authentic Gourmet was alerted by FDA sample an… | FDA 2012-07-13

FDA recall notice for Strawberry Filled Cake, 21.9 oz (1lb 6oz) (620g), UPC 3 760147 195867 (Authentic Gourmet). Reason: The recall was initiated because Authen

[Recalled] Raspberry Filled Cake, 21.9 oz (1lb 6oz) (620g), UPC 3 760147 195881 — The recall was initiated because Authentic Gourmet was alerted by FDA sample an… | FDA 2012-07-13

FDA recall notice for Raspberry Filled Cake, 21.9 oz (1lb 6oz) (620g), UPC 3 760147 195881 (Authentic Gourmet). Reason: The recall was initiated because Authent

[Recalled] Nature's Grain Garlic French Bread, 10 oz (284 g) packages, — Southern Bakeries, Hope, AR is recalling its Nature's Grain Garlic French Bread… | FDA 2012-07-13

FDA recall notice for Nature's Grain Garlic French Bread, 10 oz (284 g) packages, (Southern Bakeries, LLC). Reason: Southern Bakeries, Hope, AR is recalling its

[Recalled] Old Navy Toddler Girl Aqua Socks — The slip-on shoes have pull-on tabs on both the front and back of the foot open… | CPSC 2012-07-12

CPSC recall notice for Old Navy Toddler Girl Aqua Socks. Reason: The slip-on shoes have pull-on tabs on both the front and back of the foot open…. Issued 2012-0

[Recalled] Folding Step Stool — This recall involves 13-inch high folding step stools | CPSC 2012-07-12

CPSC recall notice for Folding Step Stool. Reason: This recall involves 13-inch high folding step stools. Issued 2012-07-12.

[Recalled] 200 Mini Lights — The recalled decorative light sets have "200 Mini Lights" and "Multi Lights, Gr… | CPSC 2012-07-12

CPSC recall notice for 200 Mini Lights. Reason: The recalled decorative light sets have "200 Mini Lights" and "Multi Lights, Gr…. Issued 2012-07-12.

[Recalled] Chicco Polly High Chair — This recall involves a range of Chicco Polly high chairs with pegs on the back… | CPSC 2012-07-12

CPSC recall notice for Chicco Polly High Chair. Reason: This recall involves a range of Chicco Polly high chairs with pegs on the back…. Issued 2012-07-12.

[Recalled] Wildwood Organic Medium Salsa , 14 oz, Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap. Product labeling reads in part:" WILDWOOD ORGANIC salsa MILD ***NET WT. 14OZ, MANUFACTURED

FDA recall notice for Wildwood Organic Medium Salsa , 14 oz, Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap.

[Recalled] Wildwood Organic Mild Salsa , 14 oz, Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap. Product labeling reads in part:" WILDWOOD ORGANIC salsa MILD ***NET WT. 14OZ, MANUFACTURED BY

FDA recall notice for Wildwood Organic Mild Salsa , 14 oz, Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap. Pr

[Recalled] Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing French in labeling), 397 mL. Pack size 6/14 oz per case. Packaged in plastic cup, sealed with film and capped with plastic cap. Product labeling reads in par

FDA recall notice for Wildwood Emerald Valley Kitchen Organic Mild Salsa - Canada (containing French in labeling), 397 mL. Pack size 6/14 oz per case. Packaged

[Recalled] Wildwood Emerald Valley Kitchen Organic Medium Salsa, 30 oz. Pack size 6/30 oz per case, 14 oz Pack size 6/14oz per case, Packaged in plastic cup, sealed with film and capped with plastic cap. Product labeling reads in part:

FDA recall notice for Wildwood Emerald Valley Kitchen Organic Medium Salsa, 30 oz. Pack size 6/30 oz per case, 14 oz Pack size 6/14oz per case, Packaged in

[Recalled] ACUSON SC2000 ultrasound systems at software versions VA20A or VA20B. Model number 10433816. The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Tr

FDA recall notice for ACUSON SC2000 ultrasound systems at software versions VA20A or VA20B. Model number 10433816. The SC2000 ultrasound imaging system is i

[Recalled] AirFlow, Infant Resuscitator, AF3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The Disposable Resuscitators with optional built-in pressure monitor is intended to provide re

FDA recall notice for AirFlow, Infant Resuscitator, AF3000 Series, Single use, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028 The

[Recalled] Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034 Product Usage: Philips X-ray System — When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D reconstruction… | FDA 2012-07-11

FDA recall notice for Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034 Product Usage: Philips X-ray System (Philips Healthcare Inc

[Recalled] Ventlab Rescue Med Infant Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory suppor

FDA recall notice for Ventlab Rescue Med Infant Resuscitator, Manufactured by: Ventlab Corporation, 155 Boyce Drive, Mockville, NC 27028. The Disposable Resu

[Recalled] Adult Resuscitator, Pro-5000 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonly associate

FDA recall notice for Adult Resuscitator, Pro-5000 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure monitor is inte

[Recalled] Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure monitor is intended to provide respiratory support in the presence of reversible apnea, commonl

FDA recall notice for Safe Spot Infant Resuscitator, Pro-1900 Series, Single Patient Use, The Disposable Resuscitators with optional built-in pressure moni