Fda ky jelly recall

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Tīmeklis2013. gada 25. janv. · Recall Status 1: Terminated 3 on April 11, 2014: Recall Number: Z-0875-2013: Recall Event ID: 64322: Product Classification: Lubricant, personal - … Tīmeklis2013. gada 25. janv. · Recall Status 1: Terminated 3 on April 11, 2014: Recall Number: Z-0873-2013: Recall Event ID: 64322: Product Classification: Lubricant, personal - …

K-Y Jelly Personal Lubricant, 4 oz. - amazon.com

TīmeklisRecalls PMA HDE Classification Standards: CFR Title 21 Radiation-Emitting Products X-Ray Assembler ... Device Name: K-Y LUBRICATING JELLY: Applicant: JOHNSON & JOHNSON PROFESSIONALS, INC. 325 PARAMOUNT DR. RAYNHAM, MA 02767 -0350 Correspondent: JOHNSON & JOHNSON PROFESSIONALS, INC. … Tīmeklis2024. gada 26. maijs · J.M. Smucker Co., Jif's parent company, issued the initial voluntary recall last week, after the Food and Drug Administration traced a salmonella outbreak to a manufacturing facility in Lexington, Ky. lore fiction

Jif peanut butter recall: Other companies

Tīmeklis2024. gada 19. sept. · Product Recall: Fixodent, KY Jelly, Opti Free & Poligrip RecallsDirect™ by Living Safely™ Entries RSS Comments RSS Hydrogen Cyanide poisoning (1) Hyperglycemia hazard (1) Illinois Department of Public Health ("IDPH") (2) Incomplete fermentation hazard (5) Ingestion hazard (1,178) Insect or animal … Tīmeklis2011. gada 16. febr. · February 16, 2011. February 16, 2011 — The US Food and Drug Administration (FDA) has issued a class II recall for Triad lubricating jelly packages with lot numbers beginning with the numbers 7 ... Tīmeklis2013. gada 8. marts · The healthcare giant, which has recalled countless products over the past three years for a variety of manufacturing and safety issues, has just pulled 2.3 million packages of K-Y Jelly. Specifically K-Y Tingling Jelly, K-Y Sensitive Jelly and K-Y SILK-E Vaginal Moisturizer and Personal Lubricant are going. Which FDA District … lore first appearance

The World Ends – J&J Recalls K-Y Jelly - Expert Briefings

K Y Jelly Lubricant: Uses, Application, Side Effects - Drugs.com

Tīmeklis2016. gada 1. febr. · Product Recall of Specific Batches of Lixisenatide (Lyxumia) Solution for Injection (S.C.) (FDA Advisory No. 2016-002) February 01, 2016 Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 10) (FDA Advisory No. 2016-108) August 22, 2016 lore film onlineTīmeklis2024. gada 19. okt. · On Oct. 19, the FDA announced that Mukilteo, Washington-based Ivar's Soup and Sauce Company had recalled 14,968 sleeves of its Kettle Classic Clam Chowder With Uncured Bacon, sold exclusively at Costco stores. The recalled soup comes in a two-pack of clear plastic cups surrounded by a cardboard sleeve. lore for the king

"Tīmeklis2024. gada 25. maijs · Class 2 Device Recall Dynarex. Facility Temperature excursions (from June 2024-August 2024) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21. Mckesson Letter Notifcations issued via USP by or by email if available by the … " - Fda ky jelly recall

Fda ky jelly recall

Center for Food Safety and Applied Nutrition 2001 FDA

TīmeklisMedical Device Recalls. FDA Home; Medical Devices; Databases - 1 result found ... Product Description. Recall Class. FDA Recall Posting Date. Recalling Firm. KY … Tīmeklis2024. gada 7. jūl. · Food recalls are removals of foods from the market that are in violation of the US Food and Drug Administration’s (FDA) regulations. FDA regulates …

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Tīmeklis2014. gada 29. jūl. · K-Y Tingling Jelly K-Y Sensitive Jelly K-Y Silk-E Vaginal Moisturizer and Personal Lubricant. BOYCOTT All Johnson & Johnson K-Y Products This is the latest in a long line of product recalls for Johnson & Johnson including Tylenol, Motrin, Benadryl, Acuvue contact lenses, the DePuy ASR hip replacement, … Tīmeklis2010. gada 23. dec. · Class 2 Device Recall Sterile Lubricating Jelly. Intended use: A patient lubricant is a device intended for medical purposes that is used to lubricate a body orifice to facilitate entry of a diagnostic or therapeutic device. 1. Allegiance, Distributed by: Cardinal Health, McGaw Park, IL 60085-6787, USA, Cat. LJT2.

Tīmeklis2024. gada 16. jūl. · Jelly Belly Recall 83317 Page Last Updated: November 14, 2024 Home Food Recalls Description: Jelly Belly Licorice Bridge Mix. Net Wt. 9 oz. (85g); 12 individual 3 oz. bags per caddy UPC: 071567981675 Manufactured by Jelly Belly Co., Fairfield, CA 94533 Jelly Belly Recall 83317 Information Tīmeklis2012. gada 3. jūl. · It is just a matter of it not being approved by the FDA. It is not that there are any safety issues, the company says. FDA warning letter leads J&J to …

Tīmeklis2024. gada 21. sept. · Kroger — which happens to be the largest grocery store chain in the U.S. — has issued a recall of nearly two dozen ready-to-eat vegetable products distributed by GHGA. According to the U.S. Food & Drug Administration’s site (FDA), the recall comes as a result of a potential listeria monocytogenes contamination within … Tīmeklis2009. gada 16. janv. · The FDA Alerts below may be specifically about Xylocaine Jelly or relate to a group or class of drugs which include Xylocaine Jelly. MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com. Following is a list of possible medication recalls, market withdrawals, alerts and warnings. Jul 21, 2024. …

TīmeklisCurrent Updates. On August 18, 2024, FDA requested healthcare providers, healthcare facility risk managers, and procurement staff to immediately stop using and discard all ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc., due to risk of bacterial contamination with Burkholderia cepacia complex. FDA’s new guidance …

Tīmeklis2024. gada 19. sept. · KY Jelly lubricant; Denture care from Polident, Poligrip and Fixodent; Curad bandages and first aid kits. If you have questions about any of these recalls, call Family Dollar at 844-636-7687... horizons at 77th reviewshttp://www.expertbriefings.com/news/the-world-ends-jj-recalls-k-y-jelly/ horizons assisted living clare miTīmeklisOn April 25, 2002, FDA announced a recall by Yoli, Inc., Chicago, Illinois, of 3,115 bags of mini jelly candies (or mini cup gel candy) because these products present a … loree\\u0027s bridal \\u0026 formalsTīmeklis2024. gada 31. maijs · KY jelly is a water-based, personal lubricant that is usually used for sexual intercourse or masturbation. Unlike petroleum or oil-based lubricants, it does not react with latex condoms, diaphragms, or sex toys. ... You may report side effects to FDA at 1-800-FDA-1088. K-Y Jelly side effects (more detail) horizons assisted living rochester nyTīmeklisCustomers were asked to return all cases of affected product in their possession. The letter included delivery confirmation and a return packing slip, return authorization … lore fitchTīmeklisFDA Recall Posting Date. Recalling Firm. Z-0873-2013 ... Z-0875-2013 - KY TINGLING JELLY Personal Lubricant. The product is packaged into 5 oz tubes with the UPC printed on it. Distributed By: McNeil-PPC Inc. 2 02/22/2013 Mc-NEIL-PPC, Inc. Z-0874-2013 - KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is … lorefree 打不开了Tīmeklis2013. gada 25. janv. · Class 2 Device Recall KY SENSITIVE TM JELLY: Date Initiated by Firm: January 25, 2013: Date Posted: February 22, 2013: Recall Status 1: Terminated 3 on April 11, 2014: Recall Number: Z-0873-2013: ... 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination … lorefree 去中心化