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. 1,080 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,080 in last 12 months

Showing 14581–14600 of 29,298 recalls

Medical DeviceMarch 18, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...

The Issue: Continuous operation at very high tube output may result in increased wear...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Ideal Implant Incorporated

Recalled Item: IDEAL IMPLANT Structured Breast Implant Recalled by Ideal Implant...

The Issue: The implants were deflating due to a piece of silicone disrupting the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Viewray, Inc.

Recalled Item: MRIdian Linac Radiation Therapy System Recalled by Viewray, Inc. Due to A...

The Issue: A discrepancy between optimization and planning forward dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Panda Infant Radiant Warmer Infant radiant warmers provide infrared heat...

The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat...

The Issue: The bedside panels and latch areas on the Giraffe Bedded Warmer and Panda...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 630 Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· Roche Diagnostics Corporation

Recalled Item: cobas e 801 immunoassay analyzer Recalled by Roche Diagnostics Corporation...

The Issue: The firm has confirmed complaints regarding signal drops on the cobas e 801...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· GE Healthcare, LLC

Recalled Item: Innova IGS 6 Recalled by GE Healthcare, LLC Due to There is a potential for...

The Issue: There is a potential for loss of the x-ray imaging function when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2019· Response Biomedical Corp.

Recalled Item: Randox Laboratories Ltd. Catalogue Number CQ5052 Recalled by Response...

The Issue: The form received three complaints related to the user obtaining a result...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Dense Bone Drill 6.0 6x16 mm Single-Pat- Product Usage: The Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Trilliant Surgical, LLC

Recalled Item: Gridlock Ankle Screw Driver Bit - Product Usage: Recalled by Trilliant...

The Issue: A screwdriver used to facilitate implant insertion and removal was found to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered RP 4.3x13 mm Single-Pat - Product Usage: The Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument Tri Channel 6.0 22 mm - Product Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Abutment Screw Retrieval Instrument RP/WP/6.0 - Product Usage: The...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Kit - Product Usage: The kit itself does Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument Hex & Tri-Ch NP/RP 22mm - Product Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Drill Tapered RP 4.3x10 mm Single-Pat - Product Usage: The Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC RP & Tri Ch Hex WP Recalled by Nobel Biocare...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

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

Class II — Potential Health HazardOngoing