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Baxter Initiates Voluntary Nationwide Recall of One Shipment of Intralipid 20% IV Fat Emulsion Due to Product Being Exposed to

05-10-2017

Baxter International Inc. announced today it is voluntarily recalling one shipment from a single lot of INTRALIPID 20% IV Fat Emulsion, 100 mL, distributed between 8/11/17 and 8/31/17 to hospitals and healthcare providers in the United States, to...

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Gadget Island, Inc. dba Gear Isle Issues Voluntary Nationwide Recall of Rhino 7 Platinum 5000, Papa Zen 3300, Fifty Shades 6000

05-10-2017

Newark, CA, Gadget Island, Inc. is voluntarily recalling Rhino 7 Platinum 5000 capsules, All LOTS, Papa Zen 3300 capsules, LOT# NSS050888, Fifty Shades 6000 capsules, all Lots, Grande X 5800 capsules, all Lots, to the consumer level. FDA analysis...

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Sid Wainer & Son® Initiates Class 1 Recall for Jansal Valley® Dried Chili De Arbol Peppers Due to Possible Health Risk

03-10-2017

Sid Wainer & Son® of New Bedford, MA is voluntarily recalling Jansal Valley® brand Dried Chili De Arbol Peppers because it does not have the proper allergens identified, being peanuts. People who have an allergy or severe sensitivity to peanuts...

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Tai Foong Usa Issues Allergy Alert on Undeclared Egg in Product

03-10-2017

TAI FOONG USA of Seattle, WA is recalling Royal Asia Shrimp Wonton Noodle Soup, because it may contain undeclared EGG. People who have an allergy or severe sensitivity to Egg or egg products run the risk of serious or life-threatening allergic...

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Intraocular Injections of a Compounded Triamcinolone, Moxifloxacin, and Vancomycin (TMV) Formulation: FDA Statement - Case of H

03-10-2017

Prophylactic use of intraocular vancomycin, alone or in a compounded drug, during cataract surgery is generally not recommended because of the risk of HORV.

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Infant Sleep Positioners: FDA Warning - Risk of Suffocation

03-10-2017

FDA reminding parents and caregivers not to put babies in sleep positioners. These products, sometimes also called “nests” or “anti-roll” products, can cause suffocation that can lead to death.

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Dean Dairy Conducts Voluntary Recall of Tampico® Brand Tropical Punch in Illinois, Indiana and Wisconsin Because It May Contain

02-10-2017

Impacts only the gallon-size Tropical Punch flavor of Tampico® bottled and distributed by Dean Dairy and sold in Illinois, Indiana and Wisconsin. All affected product has the “Best By” date of 12-27-17.

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Hong Lee Trading Inc. Issues Allergen Alert On Undeclared Milk Allergens In Vina Café Wake-Up Instant Coffee

30-09-2017

Hong Lee Trading Inc., NY, is recalling its VINA CAFÉ WAKE-UP INSTANT COFFEE MIX in 18 PACK CARDBOARD BOXES (.6 oz packs), with lot “EXP:17.MAR.2019 1T13.” because they contain undeclared milk allergens. Consumers who are allergic to milk...

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Greencore USA, LLC Recalls Egg Salad Sandwiches, Ham Salad Sandwiches, and Seafood Stuffing Because of Possible Health Risk

30-09-2017

Greencore, USA, LLC is voluntarily recalling egg salad sandwiches, ham salad sandwiches, and seafood stuffing as listed below. The products are being recalled because Listeria monocytogenes was found in environmental sampling conducted by FDA.

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Chun Yuen Trading Co. Issues Allergy Alert On Undeclared Milk

30-09-2017

Chun Yuen Trading Co. of South El Monte, California, is recalling its 12.7 oz of 4-in-1 Reishi Coffee due to a mislabeling of the outer packaging, which contains undeclared milk content. People who are allergic to milk run the risk of serious or...

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Endovascular Graft Systems: Letter to Health Care Providers - Type III Endoleaks Associated with Use

28-09-2017

Type III endoleak may require treatment with additional interventions such as re-lining, insertion of additional endograft components, or open surgical repair. Interventions to address endoleaks carry added risks for impacted patients.

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King Soopers Recalls Deli Chicken Salad Sandwich (6.8oz) Because of Possible Health Risk

27-09-2017

King Soopers said today it has recalled its chicken salad sandwiches that are sold in King Soopers and City Market stores, located in Colorado, Utah, New Mexico and Wyoming. The product may be contaminated with Listeria monocytogenes.

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UPDATE: Perform Only Contained Morcellation When Laparoscopic Power Morcellation Is Appropriate: FDA Safety Communication

30-12-2020

This update to the February 2020 safety communication provides information on the final guidance, Product Labeling for Laparoscopic Power...

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