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[Recalled] Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white, COBRAID- blue), sterile Part Number: 72202897 Product Usage: intended for use for the reattachment of soft tissue to bone — Distal part of the anch

FDA recall notice for Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white, COBRAID- blue), sterile Part Number: 72202897 Product Usag

[Recalled] Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545 Seizach Distributed in the USA by Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430. The use of external devices provides the surgeon wi

FDA recall notice for Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545 Seizach Distributed in the USA by Howmedica Osteonics Corp. 32

[Recalled] Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is an extra oral source X-ray system for dental radiographic examination and diagnosis of diseases of the teeth. — The IntraOs 70 system was found to have missing or incom

FDA recall notice for Fona Srl IntraOs 70 intra-oral x-ray system IntraOS 70 is an extra oral source X-ray system for dental radiographic examination and dia

[Recalled] BP7561 OPTI CCA-TS B-Lac Cassette (25 per box) Cassettes are consumables used in the OPTI CCA-TS Analyzer intended to be used for in vitro measurements of pH, PCOX2 PO2, lactate (lactic acid), total hemoglobin (tHb), and oxyge

FDA recall notice for BP7561 OPTI CCA-TS B-Lac Cassette (25 per box) Cassettes are consumables used in the OPTI CCA-TS Analyzer intended to be used for in vi

[Recalled] Discovery Kids™ Animated Marine and Safari Lamps — This recall involves Discovery Kids Animated Marine and Safari Lamps that featu… | CPSC 2012-07-03

CPSC recall notice for Discovery Kids™ Animated Marine and Safari Lamps. Reason: This recall involves Discovery Kids Animated Marine and Safari Lamps that featu

[Recalled] Multiple lots of cheese produced by Andante Dairy, Petaluma, CA; Sold in 5 oz to 8 oz sizes with no code date or variety information on packaged. Varieties include: Largo, a triple-creme cow's milk, and Picolo, a triple-creme

FDA recall notice for Multiple lots of cheese produced by Andante Dairy, Petaluma, CA; Sold in 5 oz to 8 oz sizes with no code date or variety information on pa

[Recalled] Romaine Lettuce tied with a rubber band — Positive field test for Salmonella | FDA 2012-07-03

FDA recall notice for Romaine Lettuce tied with a rubber band (Pacific International Marketing). Reason: Positive field test for Salmonella. Issued 2012-07-03.

[Recalled] Drager PT 4000 Phototherapy System — A routine internal quality check found that the Drager PT 4000 Phototherapy Sys… | FDA 2012-07-02

FDA recall notice for Drager PT 4000 Phototherapy System (Draeger Medical Systems, Inc.). Reason: A routine internal quality check found that the Drager PT 4000

[Recalled] Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patients breast and the imaging receptor plat

FDA recall notice for Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remov

[Recalled] Merge HEMO software. — The International Normalized Ratio (INR) value displayed in the study report do… | FDA 2012-07-02

FDA recall notice for Merge HEMO software. (Merge Healthcare, Inc.). Reason: The International Normalized Ratio (INR) value displayed in the study report do…. I

[Recalled] Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are Computed Tomography Systems that are intended to produce cross-sectional images of the body by computer reconstr

FDA recall notice for Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are Computed Tomography S

[Recalled] EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix Biopharmaceuticals Ltd. MDA blood bank, Sheba Hospital, Ramat-Gan, POB 888, Kiryat Ono 55000 Israel U.S. License No. 1603. Distributed by: Ethicon, Inc. P.O.

FDA recall notice for EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix Biopharmaceuticals Ltd. MDA blood bank, Sheba Hospital, Ramat-Gan, POB 88

[Recalled] 3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes. — Part of the lot received a lower concentration o

FDA recall notice for 3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Inten

[Recalled] Frozen Pangasius Fish, brand name T&T, in the following sizes: a. IQF 15 lbs bulk carton: 3/5 oz, 5/7 oz, 7/9 oz, 9/11 oz b. 11lbs x 2 per carton: 8/10 oz and 10 oz/up c. 2lbs x 5 per carton: 2/3 oz d. 15lbs carton: 2/3 oz

FDA recall notice for Frozen Pangasius Fish, brand name T&T, in the following sizes: a. IQF 15 lbs bulk carton: 3/5 oz, 5/7 oz, 7/9 oz, 9/11 oz b. 11lbs x

[Recalled] BD FACS 7-color Setup beads BD Biosciences, San Jose, CA 95131. BD FACS 7 color Setup Beads are for in vitro diagnostic use on BD FACSCanto or BD FACSCanto II systems. The beads are run with BD FACSCanto clinical software.

FDA recall notice for BD FACS 7-color Setup beads BD Biosciences, San Jose, CA 95131. BD FACS 7 color Setup Beads are for in vitro diagnostic use on BD FA

[Recalled] Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KKB5062-21US and KKB5080-21US. The Chorus is designed to be used as a standing and raising

FDA recall notice for Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KK

[Recalled] Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather ba

FDA recall notice for Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for si

[Recalled] MXR-35 Diagnostic X-ray High Voltage Generator manufactured by DRGEM Corporation. x-ray generator — The MXR-35 X-ray Generator's labeling did not include the certification stateme… | FDA 2012-06-29

FDA recall notice for MXR-35 Diagnostic X-ray High Voltage Generator manufactured by DRGEM Corporation. x-ray generator (Fujifilm Medical System USA, Inc.).

[Recalled] Dole brand Hearts of Romaine; Net Wt. 10 oz. UPC 71430 00956; Dole — IEH sample of Dole's Hearts of Romaine was positive for Listeria Monocytogenes | FDA 2012-06-29

FDA recall notice for Dole brand Hearts of Romaine; Net Wt. 10 oz. UPC 71430 00956; Dole (Dole Fresh Vegetables Inc). Reason: IEH sample of Dole's Hearts of

[Recalled] 21st Century Foods Soy Tempeh, packaged in 12 lb plastic bags and 8 oz containers — Product tested positive for the presence of coliforms | FDA 2012-06-29

FDA recall notice for 21st Century Foods Soy Tempeh, packaged in 12 lb plastic bags and 8 oz containers (21st Century Foods, Inc.). Reason: Product tested posit