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. 1,734 recalls have been distributed to Mississippi in the last 12 months.
Showing 47101–47120 of 49,744 recalls
Recalled Item: BREG Sterile Polar Pads Recalled by Breg Inc Due to The recall was initiated...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Cold Therapy Combination Units containing Sterile Polar Pads. 02356 Rev...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...
The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Grip which is part of the Synthes Universal Nail Recalled by...
The Issue: Synthes is initiating a voluntary recall of the Flexible Grip (Part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 14 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MCV Product Code: GCB50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPC Product Code: GMC50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 10 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 7 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 12 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 16 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH ST Product Code: GST51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...
The Issue: The Dens Instrument Set has been designed to facilitate the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Recalled by...
The Issue: Lot number 7542279, of the 45 mm Click 'X Pedicle Screw (Part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Combination Clamp/Large External Fixation System Recalled by Synthes...
The Issue: The L1 hex nuts, used to tighten the Large Combination Clamp, were oversized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.