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. 1,857 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
1,857 in last 12 months

Showing 2838128400 of 49,744 recalls

Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 250mm Straight Rod. Part of MAXIMIS Pedicle Screw Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS S. Probe. Part of MAXIMIS Pedicle Screw Spinal Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Head Holder. Part of MAXIMIS Pedicle Screw Spinal Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number:...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Rod Pusher Angled. Part of MAXIMIS Pedicle Screw Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 50mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 50mm and 5.5 x Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879 Recalled by...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Reduction B. Part of MAXIMIS Pedicle Screw Spinal Recalled...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Nut Driver 4.0 Hexa and Alignment Driver. Part Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Large Crosslink. Part of MAXIMIS Pedicle Screw Spinal...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2017· Keystone Dental Inc

Recalled Item: Multi-Unit Abutment Angled Recalled by Keystone Dental Inc Due to Abutments...

The Issue: Abutments are unable to accept the final abutment screw

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2017· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: The firm has identified that a fitting in some Slidemaker Stainer units may...

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2017· Penobscot McCrum LLC

Recalled Item: Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags) Recalled by Penobscot...

The Issue: Product may contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2017· Penobscot McCrum LLC

Recalled Item: Battered Jo-Jo Wedges / 00047 (5 lb bags) Recalled by Penobscot McCrum LLC...

The Issue: Product may contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2017· Penobscot McCrum LLC

Recalled Item: Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb bags) Recalled...

The Issue: Product may contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2017· Penobscot McCrum LLC

Recalled Item: Medium Coated Jo-Jo Wedges / 00040 (5lb bags) Recalled by Penobscot McCrum...

The Issue: Product may contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund