Monitor U.S. medical device recall enforcement reports from the FDA. Review product descriptions, recall reasons, classifications, dates, recalling firms and distribution information where the FDA provides them.
29,963 detailed records are currently available in this category.
JustRight Surgical is recalling various lots of JustRight 5mm Stapler product because they may deliver incomplete staple formation and incomplete tissue closure.
Catheters may not meet antimicrobial specification
QC results were out of range resulting in false resistant strains.
Possible drug interference when using the Trinder reaction method on multiple Cobas Analyzers. Results of Trinder tests may be falsely decreased when the tests are run with urine samples…
under certain circumstances the Cios Alpha system may freeze during a procedure.
A firmware bug causes incorrect values to be displayed for specific measured luminescence values.
GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova,…
GE Healthcare has recently become aware of a potential safety issue that may result in the loss of C-arm gantry motion capability on fluoroscopic Interventional imaging systems (Innova,…
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Insufficient seal on the outside packaging, potentially affecting the sterility of the product.
Catheters may not meet antimicrobial specification
Product was labeled as a 30cm graft, when in fact the graft in the box was a 15cm graft.
Field Safety Notification to advise of an issue that may occur involving the combination of the da Vinci Xi Drapes and Xi instruments. A pinched drape may cause a message on the Vision Cart…
Catheters may not meet antimicrobial specification
Catheters may not meet antimicrobial specification
Medical device recall records can change as the FDA receives additional information. Check the official record identifier and current FDA information before making health or product-use decisions.
Recall Lookup USA keeps the last complete source record available when an official data service is temporarily unavailable. When a source provides only a few fields, we show only those known facts rather than padding the page with generic text.
This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.
