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. 2,711 recalls have been distributed to Missouri in the last 12 months.
Showing 2841–2860 of 29,298 recalls
Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...
The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement Recalled by...
The Issue: Error code "50037" occurs on the IR-Hand Control when a MEERA-table is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal CHILDREN'S GENERAL TRACEPACK Recalled by DeRoyal Industries Inc Due...
The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint Recalled by GE...
The Issue: GE HealthCare has become aware of an issue in Centricity Universal Viewer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal C-SECTION TRACEPACK Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal is recalling certain lots of surgical procedure pack products that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE MAXORB EXTRA ALGINATE WOUND DRESSING 4X4 SQUARE Recalled by Advanced...
The Issue: Due to defects on primary packaging pouch that compromise the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hollister CalciCare Calcium Alginate Dressing calcium alginate dressings...
The Issue: Due to defects on primary packaging pouch that compromise the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Calcium Alginate Dressing MFR# 3562 Wound dressing indicated for...
The Issue: Due to defects on primary packaging pouch that compromise the device's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home Transmitter The Merlin@home" (M@h) transmitter is intended...
The Issue: Due to heart transmitter not being able to upgrade to the current software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home with the MerlinOnDemand capability Transmitter Merlin@home with...
The Issue: Due to heart transmitter not being able to upgrade to the current software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT...
The Issue: Disposable biopsy instruments were potentially manufactured missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 PSA assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The IMMULITE 2000 PSA assay for use on the IMMULITE 2000 and IMMULITE 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Flex Extenders Recalled by Westmed, Inc. Due to Due to connector within...
The Issue: Due to connector within the circuit flex extender not meeting specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMBU / KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.