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. 2,598 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,598 in last 12 months

Showing 1252112540 of 28,172 recalls

Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- SPEC0002B ARTHROGRAM TRAY SPEC0002B ARTHROGRAM TRAY SPEC0004C...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion- Pelvic Exam Kits DYNDE1037 PELVIC EXAM TRAY Recalled by Centurion...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion-LVAD Kits DM1005 DAILY LVAD MAINTENANCE KIT DM280A LVAD MANAGEMENT...

The Issue: Incomplete seals on the sterile package may compromise the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2019· bioMerieux, Inc.

Recalled Item: VIDAS Varicella Zoster IgG (VZG) antibody IVD Recalled by bioMerieux, Inc....

The Issue: Two batches of VIDAS Varicella-Zoster IgG (VZG ) may yield an invalid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2019· Abbott Medical

Recalled Item: Fast-Cath Trio HEMOSTASIS INTRODUCER Recalled by Abbott Medical Due to...

The Issue: Fast-Cath Trio Hemostasis Introducer devices contained 12F sized dilators...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2019· Abbott Medical

Recalled Item: Fast-Cath Hemostasis Introducer Recalled by Abbott Medical Due to Three lots...

The Issue: Three lots of Fast-Cath Hemostasis Introducer devices contained 8F sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & Co. KG Recalled by Karl Storz Endoscopy Due to The firm has...

The Issue: The firm has become aware that there is a potential that the glass cover at...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Stryker GmbH

Recalled Item: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part Recalled by...

The Issue: Instrument can break at the level of the thread when being exposed to high...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA bone densitometer Recalled by GE Healthcare, LLC Due to An issue...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· Johnson & Johnson Surgical Vision Inc

Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...

The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· 3-D Matrix, Inc.

Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...

The Issue: The boxes used by the shipper were not validated for use during transport.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Argon Medical Devices, Inc

Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...

The Issue: Incorrect product labeling.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Polymer Technology Systems, Inc.

Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...

The Issue: One brand of batteries have a small dimensional difference in the negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2019· Thoratec Corp.

Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...

The Issue: Excessive static electricity can potentially cause unrecoverable power loss...

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

Class II — Potential Health HazardOngoing