95,102 total recalls in our database
An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp., Morganella Morganii) when tested with doripenem, ertapenem, meropenem, imipenem, cefepime, piperacillin/tazobactam and aztreonam.
Unknown Manufacturer
The recalled products can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.
Unknown Manufacturer
A safety feature can malfunction if the laminator overheats, posing a fire hazard.
Dooya Mechanic & Electronic Tech Co., of Ningbo, China
The battery packs can overheat, posing a fire hazard.
Unknown Manufacturer
Improper installation of the fireplaces can lead to problems with heat release and/or ventilation, posing a fire hazard.
Unknown Manufacturer
The recalled clothing fails to meet flammability standards for clothing textiles, posing a risk of burn injuries to consumers.
Fudge contains undeclared tree-nuts
Product may contain foreign material: pieces of plastic
Presence of coliform found in 3rd party lab samples
Product may contain undeclared milk
Subpotent drug: Out of specification for assay at the end-of-shelf-life 24-month period.
Heritage Pharmaceuticals
Subpotent Drug
Failed dissolution specifications
Defective Delivery System: Recalled lot was found to be out of specification for shear. Shear is an attribute related to the adhesive properties of the transdermal patches.
Accelerate Diagnostics
Due improperly formulated and released bulk lot of fluorescence in situ hybridization (FISH) probes resulting in false positive identification results for Staphylococcus aureus and Streptococcus spp.
Busse Hospital Disposables
Kits containing 3M Steri-Drape Surgical Drapes recalled by 3M due to liner on the adhesive component is difficult to remove without damaging the product and may render the product unusable
The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to a potential false-negative result interpretation. The issue was identified by the firm after failing to meet lot requirements for potency. The lot release error was discovered on October 08, 2021, after a failed potency test was determined during 6-month stability evaluation of retention material for the lots. The subsequent manufacturing investigation, which included a review of the lot release potency documentation, found that the initial lot release potency test for the lot was misinterpreted.
Mobius Imaging
Stryker received a report of a battery fire involving an Airo TruCT unit previously subjected to bypass charging. The firm is notifying customers with units whose battery monitoring systems were bypassed to charge the batteries; the batteries in these units require replacing.
Primus Corporation
The Control Level I material value was showing results exceeding the upper limit of the acceptable range after a period of three (3) months. The unacceptable Control Level 1 value results in the Analyzer generating an error code which stops further testing and nullifies associated patient samples, resulting in a delay in patient results and a potential delay in therapeutic modifications.
Potential staple deployment failure and device fragment generation