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.

52,570 total recalls
2,711 in last 12 months

Showing 33213340 of 52,570 recalls

Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate Recalled by...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO...

The Issue: Due to an error message that prevents users from utilizing carboxyhemoglobin...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Physio-Control, Inc.

Recalled Item: LIFEPAK 35 ECG cable Recalled by Physio-Control, Inc. Due to Product shipped...

The Issue: Product shipped with incorrect IFU. IFU does not include proper...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2025· Microbiologics Inc

Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Control Panel...

The Issue: Internal quality control procedures were not followed correctly for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2025· Microbiologics Inc

Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel...

The Issue: Internal quality control procedures were not followed correctly for the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 17, 2025· The W.S. Badger Company, Inc.

Recalled Item: BADGER 50 Recalled by The W.S. Badger Company, Inc. Due to Labeling: Missing...

The Issue: Labeling: Missing Label: The finished product potentially missing the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJanuary 17, 2025· McKesson

Recalled Item: Inflectra (infliximab-dyyb) Recalled by McKesson Due to cGMP Deviations:...

The Issue: cGMP Deviations: Product intended for quarantine was inadvertently distributed.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 17, 2025· Zhejiang Luyao Electronics Technology Co., Ltd.

Recalled Item: Brand Name: HOMEDICS Product Name: Air Compression Leg Massager...

The Issue: Regulatory documentation error and misleading color packaging claim.

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

Class II — Potential Health HazardOngoing