Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,905 recalls have been distributed to Missouri in the last 12 months.
Showing 24441–24460 of 29,298 recalls
Recalled Item: Manual trephines are bone cutting and drilling instruments that are Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson cerebellar extensions are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Traction tong replacement screws Recalled by Instrumed International, Inc....
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement screw non-springloaded traction tongs are skull tongs for...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson braces are bone cutting and drilling instruments that are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lock nuts for titanium traction tongs are used in traction Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...
The Issue: The pediatric breathing circuits can crack prior to and during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biatain Super Non-Adhesive Recalled by Coloplast Manufacturing US, LLC Due...
The Issue: Coloplast is conducting a recall for one lot (4201931) of the Biatain Super...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...
The Issue: GE Healthcare has become aware of a potential safety issue involving missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: The software issue described was corrected in the modification to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Panoramic X-Ray System used to perform dental and orthodontic...
The Issue: Failure of the primary collimator may result in unintentional movement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 540 Indicated for use for patients from newborn Recalled by GE...
The Issue: Loss of imaging - affected devices may experience a loss of real-time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IGS 740 Indicated for use for patients from newborn Recalled by GE...
The Issue: Loss of imaging - affected devices may experience a loss of real-time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...
The Issue: Misbranding: Although the product labeling identifies the catheters as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova 4100IQ Indicated for use in generating fluoroscopic images of...
The Issue: Loss of imaging - affected devices may experience a loss of real-time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...
The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...
The Issue: Two malfunctions posing potential risk to patients were identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...
The Issue: Aerogen has received a small number of complaints in relation to the main...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.