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[Recalled] TORTUGAS QTY: 60 MEXICANTOWN BAKERY 313-894-2000 — The firm voluntarily recalled a total of 11 products: this product was recalled… | FDA 2012-05-08

FDA recall notice for TORTUGAS QTY: 60 MEXICANTOWN BAKERY 313-894-2000 (Mexicantown Wholesale). Reason: The firm voluntarily recalled a total of 11 products: t

[Recalled] Frozen Salted Clam, 12/210g. Distributed by: Seoul Shik Poom, Engleside, NJ. Origin: Republic of Korea. — Korean Certified Shippers delisted from ICSSL | FDA 2012-05-08

FDA recall notice for Frozen Salted Clam, 12/210g. Distributed by: Seoul Shik Poom, Engleside, NJ. Origin: Republic of Korea. (Seoul Shik Poom, Inc.). Reason

[Recalled] CUERNOS (CROISSANT) QTY: 90 MEXICANTOWN BAKERY 313-894-2000 — The firm voluntarily recalled a total of 11 products: this product was recalled… | FDA 2012-05-08

FDA recall notice for CUERNOS (CROISSANT) QTY: 90 MEXICANTOWN BAKERY 313-894-2000 (Mexicantown Wholesale). Reason: The firm voluntarily recalled a total of 11

[Recalled] CONCHA CHOCOLATE QTY: 90 MEXICANTOWN BAKERY 313-894-2000 — The firm voluntarily recalled a total of 11 products: this product was recalled… | FDA 2012-05-08

FDA recall notice for CONCHA CHOCOLATE QTY: 90 MEXICANTOWN BAKERY 313-894-2000 (Mexicantown Wholesale). Reason: The firm voluntarily recalled a total of 11 pro

[Recalled] MAGDALENA QTY: 54 MEXICANTOWN BAKERY 313-894-2000 — The firm voluntarily recalled a total of 11 products: this product was recalled… | FDA 2012-05-08

FDA recall notice for MAGDALENA QTY: 54 MEXICANTOWN BAKERY 313-894-2000 (Mexicantown Wholesale). Reason: The firm voluntarily recalled a total of 11 products:

[Recalled] V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for Use for the V Seri

FDA recall notice for V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use under the direc

[Recalled] Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products — Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed Handpiece | FDA 2012-05-07

FDA recall notice for Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products (MTI Precision Products LLC.). Reason: Sharp edge on the body/housing of th

[Recalled] The Brilliance iCT and iCT SP are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. These devices

FDA recall notice for The Brilliance iCT and iCT SP are Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer rec

[Recalled] USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Models AT3800 and AT4700.

FDA recall notice for USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precaution

[Recalled] CIVCO General Purpose Sensor, Non-sterile reusable general purpose electromagnetic sensor for use with 3D Guidance driveBAY, driveBAY 2, trakSTAR, or trakSTAR2 trackers, Ref. 10441627. The firm name on the label is CIVCO, Kalon

FDA recall notice for CIVCO General Purpose Sensor, Non-sterile reusable general purpose electromagnetic sensor for use with 3D Guidance driveBAY, driveBAY 2, t

[Recalled] CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose driveBAY, trakSTAR, electromagnetic sensor (8mm) with VirtuTRAX Instrument navigator and (8.9 tapered to 1.3 x 147cm) telescopically-folded CIV-Flex senso

FDA recall notice for CIVCO VirtuTRAX Instrument Navigator, Reusable non-sterile general purpose driveBAY, trakSTAR, electromagnetic sensor (8mm) with VirtuTRAX

[Recalled] BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use. — The Beauty Angel was marketed without a 510k | FDA 2012-05-07

FDA recall notice for BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human use. (JK Products & Services, Inc). Reason: The Beauty Ang

[Recalled] Frozen Cooked Oyster: 1) Cooked Oyster 40-90 CT/LB IQF Packed By: Dai One Food.Co., LTD. Country of Origin: Republic of Korea. NET WT.: 40 LBS with 8 LBS Glaze; ICSSL No. KR-8-SP 2) AquaRoyale FROZEN COOKED OYSTER IQF PACKED FOR

FDA recall notice for Frozen Cooked Oyster: 1) Cooked Oyster 40-90 CT/LB IQF Packed By: Dai One Food.Co., LTD. Country of Origin: Republic of Korea. NET WT.: 40

[Recalled] AquaRoyale Oyster IQF Packed By Dai One Food.Co., LTD. Packed For: Sunny Seafoods, Inc. 11 Sunflower Avenue, Paramus, NJ 07652. USA NET WT.: 20 LBS (40/8oz) ICSSL No. KR-8-SP — This recall was mandatory by the States | FDA 2012-0

FDA recall notice for AquaRoyale Oyster IQF Packed By Dai One Food.Co., LTD. Packed For: Sunny Seafoods, Inc. 11 Sunflower Avenue, Paramus, NJ 07652. USA NET WT

[Recalled] Half Shell Oyster Imported By: KORYEO INT'L CORP 200 STEWART AVENUE, BROOKLYN, NY 11237; SPEC 72PCS; COUNTRY OF ORIGIN: REPUBLIC OF KOREA; METHOD OF PRODUCTION: FARM RAISED; ICSSL No. KR-8-SP — This recall was mandatory by the S

FDA recall notice for Half Shell Oyster Imported By: KORYEO INT'L CORP 200 STEWART AVENUE, BROOKLYN, NY 11237; SPEC 72PCS; COUNTRY OF ORIGIN: REPUBLIC OF KOREA

[Recalled] Robotic hand accessory to InMotion Arm, rehabilitation robot. — Unsupervised patient could potentially mis-use the device and remove or rotate… | FDA 2012-05-05

FDA recall notice for Robotic hand accessory to InMotion Arm, rehabilitation robot. (Interactive Motion Technologies, Inc.). Reason: Unsupervised patient could

[Recalled] Depuy Spine Side Fire Needles 13G X 6IN, part of the Confidence Spinal Cement System Product Code 283904613. The Confidence Side Fire Needle is used to place bone cement in an intra-vertebral fashion at a desired location. t

FDA recall notice for Depuy Spine Side Fire Needles 13G X 6IN, part of the Confidence Spinal Cement System Product Code 283904613. The Confidence Side Fire

[Recalled] Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chair, room

FDA recall notice for Tabs Professional Monitor, includes one wall bracket, Model 25022. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help red

[Recalled] Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle, part of the Confidence Spinal Cement System Product Code 283904611. The Confidence Side Fire Needle is used to place bone cement in an intra-vertebral fashion at a de

FDA recall notice for Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle, part of the Confidence Spinal Cement System Product Code 283904611. The Con

[Recalled] Tabs Professional Monitor, without pull cord or wall bracket, Model 25025. Stanley Security Solutions, Inc., Lincoln, NE. Designed to help reduce the risk of falls by alerting caregivers when a resident is leaving a bed, chai

FDA recall notice for Tabs Professional Monitor, without pull cord or wall bracket, Model 25025. Stanley Security Solutions, Inc., Lincoln, NE. Designed to