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All product recalls associated with Genentech, Inc..
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Lack of Assurance of Sterility: Deformed stoppers observed during filling operations for Cathflo Activase.
Siemens Healthineers has identified an issue with the RAPIDPoint500e system software version 5.3. This issue affects how the sample source is identified at the LIS when using the capillary mode. With this software version, samples run in the capillary mode are incorrectly labeled as arterial when displayed on the LIS, leading to the potential for results to be flagged according to an established arterial range. Capillary sample results are correctly identified as capillary on both the RAPIDPoint 500e system display and the instrument printouts. The issue only affects the new software version 5.3 and only capillary sample mode is impacted. The inability to distinguish specimen sources for blood gas may lead to incorrect diagnoses and management decisions.
Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.
Cranial Caudal Blades manufactured incorrectly could result in fracture and/or damage to the bone structure
Labeling: Incorrect Lot and/or Expiration Date: The carton has incorrect expiration of 2026-MAY*, whereas the correct expiration date, which is on the tablet bottle label, is 2025-APR.
Forest River, Inc. (Forest River) is recalling certain 2024-2025 Solera, 2023-2025 Forester, and Sunseeker motorhomes. The Liquid Propane (LP) line may not be properly secured, which can cause the line to become damaged and leak.
Listeria monocytogenes identified in finished product testing.
Listeria monocytogenes identified in finished product testing.
Listeria monocytogenes identified in finished product testing.
Listeria monocytogenes identified in finished product testing.
Product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
The recall involves Super Lube products which include the following: Syncopen Synthetic Penetrant, Fire Resistant Hydraulic Fluid, and Metal Protectant and Corrosion Inhibitor. The products are used to prevent corrosion in various machinery. Super Lube Syncopen Synthetic Penetrant was sold in a four-ounce white spray bottle (item number 85004), a 32-ounce or one-quart trigger spray black plastic bottle (item number 85032), and a one-gallon (item number 85010) white plastic bottle with a handle. The container bears the brand Super Lube followed by a flag of green, blue, orange, and yellow stripes. Super Lube Fire Resistant Hydraulic Fluid was sold in a one-gallon white plastic bottle (item number 86010) with a handle. Super Lube Metal Protectant & Corrosion Inhibitor was sold in a 32-ounce or one-quart trigger spray black plastic bottle with a handle (item numbers 83032 / 83032A). The Super Lube products have one of the following lot numbers located on the bottom or rear label: Super Lube Syncopen Synthetic Penetrant Size Item Number Lot Number 1.0 Gallon Bottle 85010 17348 L24 - 23320 K26 1.0 Quart Trigger Sprayer 85032 17290 J35 - 23320 K26 4 ounce Bottle 85004 17348 L24 - 23320 K26 Super Lube Fire Resistant Hydraulic Fluid Size Item Number Lot Number 1 Gallon Bottle 86010 16120 D48 - 24040 B16 Super Lube Metal Protectant & Corrosion Inhibitor Size Item Number 1 Quart Trigger Sprayer 83032 / 83032A 17348 L24 - 23297 J49
Deep brain stimulation system will first turn off after approximately 50 days after the system is activated and subsequently, this same action will recur approximately every 50 days thereafter. This unexpected lost of stimulation may result in loss of therapy.
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
The duration between the implantable pulse generator reaching the elective replacement indicator threshold and end of service may be shorter than indicated in product labeling.
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Incorrect component placed in four manufactured lots of the TourniKwik" Tourniquet Set.