State
73,381 recalls have nationwide distribution and so reach Mississippi. 5,377 additional recalls listed Mississippi specifically in their distribution scope.
Of the 5,377 recalls naming Mississippi we have scored against our rubric, 933 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,346 (25%) are Severe.
Which agencies issued them
These figures cover only the 5,377 recalls whose distribution notice names Mississippi specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DeRoyal Industries is recalling 120 units of Biopsy Packpack medical devices distributed across 23 states. The specific reason for the recall is not disclosed in the FDA notice.
DeRoyal Industries is recalling 240 DeRoyal HEART PACK medical device kits (REF 89-8351.11). The specific reason for the recall is not disclosed in the FDA notice.
DeRoyal Industries is voluntarily recalling 51 units of the DeRoyal TOTAL HIP KIT (Lot 56187960 and 57031051) distributed to healthcare facilities across 23 US states.
DeRoyal Industries voluntarily recalled 75 units of its PACEMAKER ICD PACK (REF 89-10216.06, Lot 57898501) distributed across 23 US states on November 3, 2022.
DeRoyal Industries Inc voluntarily recalls 105 kits of DeRoyal Foot Pack (Lot 57899862, exp 3/1/2025) distributed across 23 U.S. states. Affected customers should contact the firm for recall instructions.
DeRoyal Industries voluntarily recalled 49 kits of the GEO-MED TOTAL KNEE PACK A & B distributed across 23 U.S. states. The specific reason for the recall is not detailed in the FDA notice.
DeRoyal MAJOR ORTHO PACK kits (Ref 89-9250.07) are being voluntarily recalled. The specific reason is not provided in the FDA notice. Affected lots were distributed across 23 U.S. states.
DeRoyal Industries is recalling 36 kits of the LAMI/CRANI PACK (lot numbers 56219159 and 56593562, expiring 4/1/2026) distributed across 23 US states. This is a voluntary Class II device recall; the specific reason was not disclosed in available documentation.
DeRoyal Industries initiated a voluntary Class II recall of its Lumbar Fusion Pack (51 kits) distributed across 23 US states. The specific reason for the recall was not documented in available records.
New Flyer is recalling 746 transit buses because a loose steering column connection may cause loss of steering, increasing crash risk.
BMW recalls certain 2022-2023 iX, i4, and 2023 i7 models due to a high voltage battery ECU software issue that may interrupt electrical power and suddenly disable drive power.
BMW is recalling certain 2023 X5 models because one of four bolts connecting the driver's seat backrest to the frame may not have been correctly installed, potentially preventing proper occupant restraint during a crash.
PACCAR is recalling 2015-2023 Peterbilt 320 and 520 refuse trucks because suspension brackets may fail, causing axle instability and increasing crash risk.
Lightning eMotors is recalling 2021-2022 FE4-129 vehicles because the high-voltage battery may lose traction power or fail to start, increasing crash risk.
Mercedes-Benz is recalling 2021-2022 GLE and GLS vehicles because a steering coupling locking screw may loosen, potentially causing a loss of steering control.
Mercedes-Benz is recalling 278 2022 AMG G63 vehicles because the rear axle differential housing may crack or break, potentially causing loss of control.
Hyundai is recalling 2021 Kona Electric vehicles because a defective Electric Power Control Unit may leak coolant, potentially causing a loss of drive power and increasing crash risk.
Mercedes-Benz is recalling one 2022 S 500 vehicle because the dashboard may be insufficiently attached, which can result in improper front passenger air bag deployment.
PACCAR is recalling certain 2022–2023 Peterbilt 579 vehicles because the molded hood mirror assemblies may break at the pivot joint and fall into the roadway, creating a road hazard.
Mercedes-Benz is recalling 2019 AMG GT53 and GT63 vehicles because the center console may unlatch during a crash, increasing injury risk.
Mountain View Packaging is recalling frozen Crispy Chicken with Almonds entrée due to undeclared shrimp, a known allergen. No adverse reactions have been reported.
Gyroor C3 e-bikes are recalled because the battery pack can ignite, creating fire and burn hazards. Gyroor has received reports of battery packs igniting and injuries requiring medical treatment, including burns and smoke inhalation.
General Motors recalls 2017-2023 Chevrolet Bolt EV vehicles. After a crash with pretensioner deployment, pretensioner exhaust may ignite carpet near the B-pillar, creating a fire hazard.
Ridewell is recalling certain 266 Suspensions with Haldex Air Disc Brakes because a retaining clip may detach, reducing brake performance or causing a flat tire.
Samnyte Tattoo Numbing Cream is recalled because its packaging does not meet child-resistant requirements under federal law. The product contains lidocaine and poses a poisoning risk if ingested by young children.