State

Mississippi product recalls

73,596 recalls have nationwide distribution and so reach Mississippi. 5,379 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total: 5,379
Critical: 931
Severe: 1,349
Most recent: 2026-10-24

Of the 5,379 recalls naming Mississippi we have scored against our rubric, 931 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,349 (25%) are Severe.

Which agencies issued them

These figures cover only the 5,379 recalls whose distribution notice names Mississippi specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26476–26500 of 78975

HighFDA (Devices)·Z-1708-2021·2021-06-09
ZVplasty Bone Access Kit Recalled for Inadequate Sterilization
Zavation has recalled the ZVplasty Direct Unipedicular Bone Access Kit with Drill due to potential sterilization failure. The surgical device is used in orthopedic and spinal procedures, with 11 units distributed nationwide.
Product
ZVplasty Direct Unipedicular Bone Access Kit with Drill, 10 Gauge, REF VCF-DSBAK. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1762-2021·2021-06-09
Zavation ZVplasty Orthopedic System Recalled for Inadequate Sterilization
Zavation's ZVplasty System surgical devices may not have been adequately sterilized, creating infection risk. The recall affects 195 units distributed nationwide in the US across multiple lot numbers.
Product
ZVplasty System, 15mm, Part Numbers: a) VCF-1015-2 b) VCF-1015-2A. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0634-2021·2021-06-09
Clio No Added Sugar Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio No Added Sugar Yogurt Bars (Mixed Berry/Peach, 50g) due to possible metal fragments in the product. Approximately 1,880 units were distributed nationwide.
Product
Clio No Added Sugar Yogurt Bar Mixed Berry / Peach 50g x 16 (12pc tray). UPC Code: 854021008220
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1761-2021·2021-06-09
Spinal surgery implant kit recalled for inadequate sterilization
Zavation is recalling ZVplasty 10G spinal implant kits that may not have been properly sterilized. The affected devices were distributed nationwide and may pose infection risk if implanted.
Product
ZVplasty 10G, 15mm, Additional Level Kit, REF VCF-1015-1A. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0635-2021·2021-06-09
Clio Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Greek Yogurt Bar Vanilla/Strawberry Club pack 50g x 12, 16pc tray due to possible metal fragments in the product. Consumers should not consume the affected product.
Product
Clio Greek Yogurt Bar Vanilla / Strawberry Club pack 50g x 12 , 16pc tray. UPC Code: 854021008121
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0602-2021·2021-06-09
Buspirone Hydrochloride Tablets Recalled for Foreign Tablet Contamination
Oxford Pharmaceuticals is recalling 6,864 bottles of Buspirone Hydrochloride Tablets, 15 mg, distributed nationwide due to the presence of foreign tablets or capsules in the product.
Product
BUSPIRONE HYDROCHLORIDE — BUSPIRONE HYDROCHLORIDE (BUSPIRONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1774-2021·2021-06-09
Philips BRILLIANCE VOLUME CT System cooling unit may eject from gantry
A cooling unit in the Philips BRILLIANCE VOLUME computed tomography system may unexpectedly eject from the gantry, posing a risk of injury. Two affected units are being recalled.
Product
BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended to produce images of the head and body. Model Number: 728306
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1714-2021·2021-06-09
Zavation Orthopedic Stylet Recalled for Inadequate Sterilization
Zavation is recalling 56 units of 10 gauge direct unilateral stylets used in spinal procedures because products distributed as sterile may not have been adequately sterilized. Affected units were distributed nationwide.
Product
10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKbd. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1717-2021·2021-06-09
Orthopedic spinal implants recalled due to inadequate sterilization
Zavation is recalling 7 units of 11G DIRECT SINGLE spinal implants (lots 2001185 and 2001243) because products distributed as sterile may not have been adequately sterilized. The devices were distributed nationwide.
Product
11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) CODE: INTVMN-SCDK. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1743-2021·2021-06-09
10G Direct Single Bone Access Kits recalled for sterilization failure
Zavation's 10G Direct Single Bone Access Kits are being recalled because products distributed as sterile may not have been adequately sterilized, posing infection risk in orthopedic procedures.
Product
10G DIRECT SINGLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1773-2021·2021-06-09
Change Healthcare Enterprise Viewer software defect affects image display settings
A software defect in Change Healthcare Enterprise Viewer versions 2.0 and 2.1 prevents the display of image presentation styles. The viewer is used nationwide for displaying medical images.
Product
Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware for the 2D and 3D display of DICOM and non-DICOM medical images, reports, and multimedia content.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0647-2021·2021-06-09
Lipodrene With 25mg Ephedra Extract recalled for unapproved food additive
Hi Tech Pharmaceuticals is recalling Lipodrene With 25mg Ephedra Extract because the product contains 1,4-dimethylamylamine (DMAA), an unapproved food additive.
Product
Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
Category
Drug
Distribution
38 states
ModerateFDA (Devices)·Z-1695-2021·2021-06-09
K2M Cascadia AN Interbody Implants Recalled for Mislabeled Dimensions
K2M, Inc is recalling Cascadia AN Interbody Convex lumbar implants with mislabeled product dimensions. The affected sizes include 10x22x14mm, 10x28x14mm, and 10x22x15mm. No injuries have been reported.
Product
Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2 Lumbar implants are intervertebral body fusion devices indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as anadjunct to…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0601-2021·2021-06-09
Thiamine HCl Injection Recall: Vials with Incorrect Lot Numbers
Mylan Institutional LLC is recalling Thiamine Hydrochloride Injection USP 200 mg/2 mL due to vials labeled with incorrect lot numbers. The cartons contain the correct lot number 200906 but vials inside are labeled with lot number 200901.
Product
THIAMINE HYDROCHLORIDE — THIAMINE HYDROCHLORIDE (THIAMINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·21V435000·2021-06-08
Land Rover Defender Recalled for Rear Light Assembly Failure Risk
Jaguar Land Rover is recalling 2020-2022 Defender X vehicles with smoked rear lights because a voltage spike can cause turn signals and brake lights to fail.
Product
LAND ROVER — LAND ROVER DEFENDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E050000·2021-06-07
One More Auto Parts Recalls Lasfit Headlight Bulbs for Excessive Brightness
One More Auto Parts is recalling Lasfit headlight bulbs that are too bright during the first ten minutes of use, posing a crash risk.
Product
EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V433000·2021-06-07
Coach House Platinum Recalled for Potential Gas Leak in Cooking Stove
Coach House is recalling 2021 Platinum vehicles because an overtightened bolt on the cooking stove may damage the seal, causing a gas leak that increases fire risk.
Product
COACH HOUSE — COACH HOUSE PLATINUM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V432000·2021-06-07
2022 Honda Odyssey Second-Row Seat Frames May Unlock Unexpectedly
Honda is recalling 2022 Odyssey vehicles because second-row outboard seat frames have deformed locking mechanisms that may prevent them from locking into place. Unlocked seats could move unexpectedly, increasing injury risk.
Product
HONDA — HONDA ODYSSEY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V430000·2021-06-04
Highland Ridge RV Recalls Trailers with Propane Regulator Defect
Highland Ridge RV is recalling certain 2019-2021 fifth wheel and travel trailers because a propane regulator may fail, increasing fire risk.
Product
HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, HIGHLAND RIDGE TT OPEN RANGE, SILVERSTAR, MESA RIDGE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V426000·2021-06-04
KZRV Sidewinder Recalled for Propane Regulator Fire Risk
KZRV is recalling 2018-2019 Sidewinder RVs because a propane regulator may fail, increasing pressure and fire risk.
Product
KZRV — KZRV SIDEWINDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V425000·2021-06-04
Jayco travel trailers and fifth wheels recalled for propane regulator failure fire risk
Jayco is recalling approximately 87,649 certain 2017-2021 travel trailers and fifth wheels with defective Winntec propane regulators that may fail and increase fire risk.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER PINNACLE, OCTANE, NORTH POINT, JAY FLIGHT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V431000·2021-06-04
Starcraft RV Recalls Travel Trailers and Fifth Wheels Due to Propane Regulator Defect
Starcraft RV is recalling specific 2017-2021 travel trailers and fifth wheels because a propane regulator may fail, increasing fire risk.
Product
STARCRAFT RV TT — STARCRAFT RV TT, STARCRAFT RV FW AUTUMN RIDGE, AR-ONE MAXX, MOSSY OAK, AUTUMN RIDGE OUTFITTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V429000·2021-06-04
Trails West Sierra Trailer Recall for Gas Leak Risk
Trails West is recalling one 2020 Sierra 4H 15x19 LQ trailer due to a potential gas leak from the stove that could increase fire risk.
Product
TRAILS WEST — TRAILS WEST SIERRA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V427000·2021-06-04
Keystone Recalls 2019-2020 RVs Due to Propane Regulator Fire Risk
Keystone is recalling 2019 Bullet and Sprinter and 2020 Hideout RVs because a propane regulator may fail, increasing fire risk.
Product
KEYSTONE — KEYSTONE HIDEOUT, BULLET, SPRINTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V428000·2021-06-04
Recreational vehicles recalled for propane regulator failure and fire risk
Heartland and Cruiser recreational vehicles with defective Winntec propane regulators may experience increased pressure, enlarging gas-appliance flames and increasing fire risk. Dealers will replace the regulator free of charge.
Product
HEARTLAND — HEARTLAND, CRUISER RV, CRUISER SUNDANCE, TRAIL RUNNER, LITHIUM, PROWLER
Category
Vehicle
Distribution
Distributed nationwide