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All product recalls associated with Sendx Medical Inc.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
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.
Error in the Ca12 calibration value for pCO2 recorded in the cal pack barcode for lot 17323. This error will result in falsely elevated pCO2 results at the high end of the measuring range.
Smith Medical has become aware that an increase in pH may occur with some medications when instilled in the Affected Cassettes. Also, a small number of catheter occlusions have been reported from one customer when these Affected Cassettes have been used for delivering Flolan.
Smith Medical has become aware that an increase in pH may occur with some medications when instilled in the Affected Cassettes. Also, a small number of catheter occlusions have been reported from one customer when these cassettes have been used for delivering Flolan.
Mislabeling: Product is labeled with the wrong expiration date: 2009-12. The correct expiration date is 2008-12.
The carbon or aluminum bicycle forks were sold on Cannondale mountain bicycle models listed below: Bicycle model code, product Retail price Lefty Speed Carbon SL 2007 Taurine Carbon Team Replica 2007 Scalpel 1 2007 Scalpel Team Replica 2007 Rush Carbon 1 2007 Rush Carbon Team 2007 aftermarket, replacement Lefty Speed Carbon SL forks $5500 $5000 $5500 $6000 $6500 $1400 Lefty Speed DLR 2 (including bonded, 100mm and 80mm) 2007 Rush Carbon 2 (This model also included in the recall for Cranksets - CPSC press release #07-206) 2007 Rush 3 2007 Rush 4 2007 Rush 5 2007 Caffeine 29'er 2007 Scalpel 2 2007 Scalpel 3 2007 Caffeine 1 2007 Caffeine 2 2007 Rush Feminine 1 2007 aftermarket, replacement Lefty Speed (bonded, 100mm and 80mm) DLR 2 2008 Rush Carbon 3 $4500 $2600 $2100 $1700 $1600 $3500 $2600 $2200 $1600 $2000 $950 $3500
Reduced Shock- the device may deliver 100 Joule (J) to a patient, which is less than the recommended factory minimum default setting of 200 J.
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
Model J Series dry fire sprinklers come in pendent, upright, and sidewall configurations. The name "Globe," the letter "J" and the year of manufacture (1990 though 1999) are embossed on the frame of each sprinkler. These dry sprinklers were designed to be installed in areas of buildings where the sprinklers or water supply pipes may be subject to freezing, such as unheated attics, freezers and coolers, parking garages, porches and warehouses.
Lack of assurance of sterility, in that the product is labeled as sterile but the package may not have been sealed.
X-ray systems were not configured to display Air Kerma Rate and Cumulative Air Kerma.
The ECG signal may become unusable to assess patient condition and need for therapy.
This voluntary recall has been initiated due to the product puncturing the packing during rough handling. Once the packaging is damaged, the product is no longer sterile as labeled.
This voluntary recall has been initiated due to the product puncturing the packing during rough handling. Once the packaging is damaged, the product is no longer sterile as labeled.
This voluntary recall has been initiated due to the product puncturing the packing during rough handling. Once the packaging is damaged, the product is no longer sterile as labeled.
Incorrect results: Falsely elevated Troponin values have been reported which are inconsistent with the patient's clinical picture and test negative by other Troponin assays.
The tip may separate from the probe.
The recalled cribs are part of the Nursery-in-a-Box furniture set which also includes a changing table and clothing organizer. The cribs are cherry, white or natural in color. Only model numbers 8910 and 8050 with serial numbers 3005 HY through 0806 HY are included in this recall. The model and serial numbers are printed on an envelope permanently attached to the mattress support. "Simplicity," model and serial numbers are also printed on a label on the bottom rail of the headboard.