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Showing 4381–4400 of 92420 results

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Little Leaf Southwest Salad Kit (Little Leaf) – incorrect dressing (2025)

Undeclared Allergen

Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.

FDAFeb 28, 2025CT, MA, NH• LITTLE LEAF FARMS LLC

Carvedilol Tablets 25mg (Glenmark) – Nitrosamine Risk (2025)

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

Class IIModerate

FDAFeb 28, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

Duloxetine Capsules 60mg (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDAFeb 28, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Carvedilol Tablets 12.5mg (Glenmark) – Nitrosamine Risk (2025)

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

Class IIModerate

FDAFeb 28, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

Walgreens Acne Control Cleanser (Sigan) – Benzene Contamination (2025)

Chemical Contamination: Presence of benzene

Class IIModerate

FDAFeb 28, 2025Nationwide• Sigan Industries Group Inc.

Carvedilol Tablets 3.125mg (Glenmark) – Nitrosamine Risk (2025)

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

Class IIModerate

FDAFeb 28, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

Duloxetine Capsules 30mg (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Class IIModerate

FDAFeb 28, 2025Nationwide• Breckenridge Pharmaceutical, Inc.

Mercedes-Benz Sprinter 2500 (Mercedes-Benz) – Parking Brake Fault (2025)

Daimler Vans USA, LLC (DVUSA) is recalling certain 2024 Mercedes-Benz Sprinter vehicles. The parking brake cable bracket welds may fail and disengage the parking brake. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 105, "Hydraulic and Electric Brake Systems."

NHTSAFeb 28, 2025Nationwide• MERCEDES-BENZ

Ford Mustang Mach E (Ford) – Battery Management Problem (2025)

Ford Motor Company (Ford) is recalling certain 2021-2022 Mustang Mach-E vehicles previously repaired incorrectly under recall number 22V-412. The high voltage battery main contactors may overheat.

NHTSAFeb 28, 2025Nationwide• FORD

Carvedilol Tablets 6.25mg (Glenmark) – Nitrosamine Risk (2025)

CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit

Class IIModerate

FDAFeb 28, 2025Nationwide• Glenmark Pharmaceuticals Inc., USA

FilmArra Pneumonia Panel (BioFire) – Test Result Reliability (2025)

Increased risk of control failures and false negative test results with multiplexed nucleic acid test.

FDAFeb 27, 2025Nationwide• BioFire Diagnostics, LLC

P.J. Salvage Pajama Sets (Unknown) – burn hazard (2025)

This recall involves P.J. Salvage Kids Checker Plush Short Sets, Fleece Pajama Sets, Smiley Plush Robes and Tie Dye Plush Sets. The Girl's Checker Plush Short Set, model RP3KHST, is a pullover hoodie with a kangaroo pocket, long pants and shorts, and was sold in gray with stars and lilac with checkers. The Kid's Fleece Pajama Set, model RP3KPST, is a pullover crew with a kangaroo pocket and jogger pants and was sold in a multi color tie dye pattern. The Girl's Smiley plush robe, model RP3KPR, is a hooded robe with front pockets and a waist tie and was sold in pink lilac with smiley faces. The Girl's Plush sets, model RP3KFST, is a fleece set with a pullover crew top and jogger pants and was sold in lilac ice with a "Smile" graphic on the front, in multi color with a "Good Vibes" graphic on the front and in sky blue with a "Sunshine" graphic on the front. They were sold in children's sizes S-XL. The sizes and "P.J. Salvage" are printed on the neck label. The side seam label has care instructions, fiber content, and country of origin information.

CPSCFeb 27, 2025Nationwide

Forever 21 Children's Pajamas (Unknown) – burn hazard (2025)

This recall involves 20 different styles of Forever 21 children's pajamas: eight pant styles, three short styles and nine two-piece pajama set styles. The pajamas were sold in children's sizes 5/6, 7/8, 9/10, 11/12 and 13/14. The size and "Forever 21" are printed on the red, black or pink label at the neck or waist of the pants and shorts. The pajamas have the following item number located on a sewn-in, side-seam label below the bar code: Pajama Product Item number White pants with pink bows 01298115 Black and white Minnie Mouse polka dot boxer shorts 01287805 Minnie Mouse white cami and print pants 01287794 Hello Kitty pink and blue stripes shirt and shorts 01299151 Black, gray and white plaid pants 01298112 Blue plaid shorts 01285181 Lavender and pink plaid shirt and shorts 01323034 Cream with teddy bear print pants 01298113 Beetlejuice print pants 01322007 Gray Beetlejuice print shirt and pants 01323269 Mickey Mouse print pants 01297198 Dalmatian print pants 01322009 Red plaid pants "Be Mine" pink and red hearts tee and shorts 01249379 "Just keep Growing" white cami and floral shorts 01261320 "Too Cute" white t-shirt and floral Shorts 01263030 Pink Hello Kitty print cami and shorts set 01274432 Sanrio Keroppi print tee and shorts 01274433 White and blue floral shorts 01285168

CPSCFeb 27, 2025Nationwide

t:slim X2 Insulin Pump (Tandem Diabetes) – Software Defect (2025)

A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.

FDAFeb 27, 2025AZ, CA, CO +26 more• Tandem Diabetes Care, Inc.

NexGen LPS Flex Knee Joint (Zimmer) – Labeling Compatibility Error (2025)

The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.

FDAFeb 27, 2025Nationwide• Zimmer, Inc.

Prestige and Aerco Esteem Gas Boilers (Triangle Tube) – CO poisoning risk (2025)

The recalled Prestige Solo, Prestige Excellence, and Aerco Esteem boilers are wall-hung condensing gas boilers housed in a white metal box. "Prestige" is printed on the white front panel of the recalled Prestige Solo and Prestige Excellence boilers. "Aerco" is printed on the front of the recalled Esteem boilers. Please visit the Triangle Tube recall website for directions on identifying if you have a recalled boiler by serial number, which can be located either on the Boiler Rating Label located on the white front panel, on a panel on the right hand side of the boiler, or behind the boiler front door. The following models and serial number ranges are included in this recall. Product Name Item Code Product Description Serial Number Range Start Serial Number Range End Date of Manufacture Prestige Solo - PA PA110 Prestige Solo PA Series PA044936 PA147874 PA155 Prestige Solo PA Series PA045337 PA147522 PA175 Prestige Solo PA Series PA044728 PA148532 PA250 Prestige Solo PA Series PA044768 PA149487 PA299 Prestige Solo PA Series PA045398 PA146746 PA399 Prestige Solo PA Series PA045420 PA148752 PA80 Prestige Solo PA Series PA044058 PA139939 Dec 2015 - Apr 2019 Prestige Solo PT PT110 Prestige Solo PT Series PT0000110 PT0053558 PT110 Prestige Solo PT Series PTA002845 PTA037637 PT110LP Prestige Solo PT Series PT0000928 PT0053557 PT110LP Prestige Solo PT Series PTA002645 PTA002764 PT175 Prestige Solo PT Series PT0002849 PT0053776 PT175 Prestige Solo PT Series PTA003087 PTA037557 PT250 Prestige Solo PT Series PT0002588 PT0053319 PT250 Prestige Solo PT Series PTA003207 PTA037467 PT399 Prestige Solo PT Series PT0005962 PT0052417 PT399 Prestige Solo PT Series PTA003388 PTA037377 PT399HP Prestige Solo PT Series PT0010893 PT0052394 PT399HP Prestige Solo PT Series PTA003496 PTA097961 PT60 Prestige Solo PT Series PT0002188 PT0051954 PT60 Prestige Solo PT Series PTA002810 PTA008253 Dec 2011 - Dec 2015 Prestige Excellence - PTE PTE110LP Prestige Excellence PT PT0001588 PT0053690 PTE110LP Prestige Excellence PTE PTE030446 PTE030479 PTE110 Prestige Excellence PT000568 PT0053624 PTE110 Prestige Excellence PTEA PTA002889 PTA003086 PTE110 Prestige Excellence PTE PTE049177 PTE049177 Dec 2011 - Dec 2015 Prestige Excellence - PEA PEA110 Prestige Excellence PEA PEA078169 PEA143958 Dec 2015 - Apr 2019 Aerco Esteem PT399ES Aerco Esteem AE1100 AE1236 PT399HP Aerco Esteem AE1237 AE1239 DF48650G/BK/P DF48650G/BK/P/LP DF48650G/S/P Dec 2011 - Dec 2015

CPSCFeb 27, 2025Nationwide• Burnsen SA, of Belgium

Access Vitamin B12 Reagent (Beckman Coulter) – Result Accuracy (2025)

Beckman Coulter has received complaints of erroneous Vitamin B12 results when using Access Vitamin B12 Reagent lot 439850. The affected reagent lot may cause erroneously low or high Vitamin B12 results, leading to a delayed or improper diagnosis and/or repeat testing.

FDAFeb 27, 2025Nationwide• Beckman Coulter, Inc.

Fleetwood Southwind (Fleetwood) – Exhaust System Issue (2025)

REV Recreation Group (REV) is recalling certain 2022-2025 Fleetwood Bounder, Flair, Fortis, Holiday Rambler Admiral, Invicta, Vacationer, 2023-2025 Fleetwood Flex, Holiday Rambler Eclipse, and 2022-2023 Fleetwood Southwind motorhomes. The engine exhaust tip may detach, allowing exhaust fumes to enter the cabin.

NHTSAFeb 27, 2025Nationwide• FLEETWOOD

Tandem Mobi Insulin Pump (Tandem Diabetes) – Software Defect (2025)

A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.

FDAFeb 27, 2025AZ, CA, CO +26 more• Tandem Diabetes Care, Inc.

MyDay Toric Contact Lenses (CooperVision) – Incorrect Cylinder Power (2025)

a limited number of lots were manufactured with an incorrect cylinder power.

FDAFeb 27, 2025CA, CO, FL +12 more• CooperVision, Inc.

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