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147 reported ongoing
147 records in this archive. Latest source date Aug 10, 2026.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Class IReported ongoing
Distribution: Domestic: IL, NC, VA, WY;
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Class IReported ongoing
Distribution: Domestic: IL, NC, VA, WY;
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Class IReported ongoing
Distribution: Domestic: IL, NC, VA, WY;
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Class IReported ongoing
Distribution: Domestic: IL, NC, VA, WY;
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
Class IReported ongoing
Distribution: US Nationwide distribution in the state of NE.
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of NE.
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MS, TX.
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
Class IIReported ongoing
Distribution: U.S. Nationwide distribution in the state of California.
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the prod...
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA.
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the prod...
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA.
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the prod...
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA.
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of California.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of Iowa.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 147 records, including 147 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.