Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,591 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,591 in last 12 months

Showing 1404114060 of 28,172 recalls

Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 11, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...

The Issue: The staplers may have an insufficient firing stroke to break the washer and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 10, 2019· Uromedica Inc.

Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...

The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...

The Issue: The firm has become aware of a potential problem that their Catheters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...

The Issue: The firm has become aware of a potential problem that their Catheters may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2019· Becton Dickinson & Company

Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...

The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...

The Issue: Product with incorrect shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Microbiologics Inc

Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...

The Issue: Product with incorrect shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...

The Issue: In affected Artis systems the movement of the floating tabletop may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount Recalled...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Recalled by...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Compass Health Brands (Corporate Office)

Recalled Item: MediPress pneumatic compression system Recalled by Compass Health Brands...

The Issue: Product design change did not receive proper premarket clearance and lacks a...

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

Class II — Potential Health HazardOngoing