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. 1,014 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,014 in last 12 months

Showing 27101–27120 of 52,570 recalls

Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX PST04089 SLEEVE AIWA CLINIC Item Number:PST04089 SLEEVE AIWA CLINIC...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VATS1SCDX DO ZABIEGOW VATS Product Usage: The Endo GIA Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm- 3.5mm(...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VMIN ZESTAW DO VATS PODSTAWOWY Product Usage: The Endo Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Recalled by...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm - Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: SLEEVEGK1 ZESTAW DO ZABIEGOW SLEEVEX1 Product Usage: The Endo GIA Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm - Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VWR ZESTAW DO VATS KLIN Product Usage: The Endo Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 60mm -2.5mm...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX SLEEVEGK3 (2) BOX SLEEVEGK4 SLEEVE GASTRECTOMY (3)BOX SLEEVEJAWI...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX HEMIGX1 ZESTAW DO HEMICOLECTOMII (Item Number HEMIGX1 ZESTAW DO...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...

The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX PST01199 BARIATRIC TRISTAPLE (Item Number: PST01199) (2) BOX PST03403...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: MGBX ZESTAW GB LS X1 Product Usage: The Endo GIA Recalled by COVIDIEN...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)LAPBARLECZNA ZESTAW BARIATRYCZNY LECZNA (2) KITBAR021- BARIATRIC KIT X1...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX BOX1073180 APPE1 APPENDIX KIT ZAMS (Item Code BOX1073180) Recalled...

The Issue: Device may be missing a sled component. The sled component is responsible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing