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All product recalls associated with Novo Nordisk Inc.
Total Recalls
1000
Past Year
726
Class I (Serious)
175
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.
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
Queso Cheese dip may contain foreign material (metal).
Temperature Abuse: product samples were stored at temperatures below 32* F which is not in accordance with storage requirements that could cause a lack of efficacy and damage to the cartridge and pen-injectors.
Presence of plastic in bagged frozen peppers and onions.
Users may observe additional locus specific signals at 9q34. The device pack insert indicates the probe has no known cross-reactivity to 9q34.
Undeclared hazelnut in Chocolate Truffles cake topping.
The firm discovered through customer complaints that device segments may not meet specifications.
Discrepancy in labeling between the adult CBC reference ranges presented in the OLO Operator's Manual and the OLO software
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the identification of Neisseria contributing to a delay in time to definitive diagnosis or a delay in proper treatment
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and reduce the identification of Neisseria contributing to a delay in time to definitive diagnosis or a delay in proper treatment
Positive Control may run high out of its assigned ISR range and result in an invalid run and necessitate retesting
This recall involves HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses sold in twin, twin XL, full, queen, and king sizes. They are 10-inch, single-sided mattresses with white knit ticking, a blue striped wave design and diamond-shaped quilting on the top surface. The side panels have gray knit ticking. The tape edges are white with white stitching. The bottom panel has gray non-woven ticking. The mattresses have a white tag located on the underside of the head panel of the mattress with "Made For HOFISH Inc." printed on one side and "Prototype ID: HF19HY" printed on the other side. Only mattresses with the Prototype ID HF19HY on the product's labeling are included in this recall. The mattresses were sold compressed in a box.
The shelf box identifies a small device actually contains a large device, and the shelf box identifying a large device actually contains a small device.
Keystone RV Company (Keystone) is recalling certain 2021 Cougar 29MBS, 30RLS, 315RLS, 316RLS, 32BHS, 353SRX, 364BHL, and 368MBI trailers equipped with the Off the Grid (OTG) Solar package. The inverter may have been incorrectly wired, causing power to energize the shore power connection, when in use.
Stryker identified non-conforming instruments that are components of the Tritanium X TL sets. The firm found non-conformances with the TL Inserter, TL Draw Rod, Tube Set/Syringe Adapter Assembly, and Syringe Plunger that could lead to device failure during a procedure.
Verification and validation of the virus transport medium tubes was not provided to FDA prior to sale and marketing