State

Mississippi product recalls

72,969 recalls have nationwide distribution and so reach Mississippi. 5,349 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total: 5,349
Critical: 923
Severe: 1,126
Most recent: 2026-09-09

Of the 5,349 recalls naming Mississippi we have scored against our rubric, 923 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,126 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,349 recalls whose distribution notice names Mississippi specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6301–6325 of 78318

SevereFDA (Drugs)·D-0482-2025·2025-07-02
Tirzepatide Injections Recalled for Lack of Sterility Assurance
Thrive Health Solutions is recalling Tirzepatide Injections (10mg/mL, pre-filled syringes) distributed nationwide due to lack of assurance of sterility. Consumers should not use the affected product and contact their healthcare provider.
Product
Tirzepatide Injections, 10mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1904-2025·2025-07-02
Broselow Pediatric Emergency Rainbow Tape recalled for incorrect dosing values
SunMed Holdings is recalling Broselow Pediatric Emergency Rainbow Tape due to incorrect values printed on the tape that could lead to improper medication dosing and defibrillation in pediatric emergency care.
Product
Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife); REF 7700REA AirLife brand, 2025 Edition, and 36-23446 Rev 2 Print Version The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0491-2025·2025-07-02
Sodium Chloride Injection Recalled for Sterility Assurance Defect
B Braun Medical Inc. is recalling 187,656 containers of 0.9% Sodium Chloride Injection USP due to potential sterility failures caused by pinholes in finger boxes during manufacturing. The defect may allow leaks and compromise the sterile nature of the intravenous medication.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1958-2025·2025-07-02
Extended Tip Applicator 8CM distributed by Integra LifeSciences recalled nationwide
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices due to potentially out-of-specification endotoxin levels and lack of sterility assurance. The recall affects 6,216 units distributed across the US and internationally.
Product
Extended Tip Applicator, 8CM, Box of 5.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0484-2025·2025-07-02
Tirzepatide Injections recalled due to lack of sterility assurance
Thrive Health Solutions is recalling Tirzepatide Injections 30mg/mL pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.
Product
Tirzepatide Injections, 30mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1961-2025·2025-07-02
MicroMyst Applicator recalled due to lack of sterility assurance
Integra LifeSciences Corp. is recalling the MicroMyst Applicator Box of 5 due to lack of sterility assurance. The product is used with the Integra Flow Source for controlled application of two liquids.
Product
MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0494-2025·2025-07-02
Ketorolac Tromethamine Ophthalmic Solution Recalled for Sterility Risk
Apotex Corp. is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% due to lack of assurance of sterility. The recall affects 87,840 bottles distributed nationwide.
Product
KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0473-2025·2025-07-02
Metoclopramide Tablets Recalled for Presence of Foreign Tablets
Teva Pharmaceuticals USA, Inc. is recalling Metoclopramide Tablets, USP 10 mg due to the presence of foreign tablets or capsules in the product. The affected lot is distributed nationwide.
Product
METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2024-2025·2025-07-02
PRIMA 2MM Eccentrical Adaptor With Screw Sterile Medical Device
Limacorporate is recalling PRIMA 2MM Eccentrical Adaptor With Screw sterile devices because the black laser marking used to identify position may be missing.
Product
PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2028-2025·2025-07-02
REMISOL Advance Medical Device Software Defect Affecting Reference Range Calculations
A software issue in REMISOL Advance may incorrectly process date-of-birth information from laboratory systems, causing incorrect reference range calculations and potentially auto-validating erroneous test result flags. The actual test results are not changed, but their evaluation may be affected.
Product
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164; C44703; C57017; C69412; C69413; C73942; C73941; C88470; C88471 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 con
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2025-2025·2025-07-02
PRIMA 4MM Eccentrical Adaptor With Screw Medical Device Recall
Limacorporate S.p.A is recalling PRIMA 4MM Eccentrical Adaptor with Screw devices because the black laser marking used to identify positioning may be missing. The defect could affect proper device placement during use.
Product
PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2000-2025·2025-07-02
BD Insyte Autoguard BC Winged IV Catheter Needle Retraction Issue
Becton Dickinson is recalling a specific lot of BD Insyte Autoguard BC Winged IV catheters (REF 382633, Lot 4222721) due to reports that the catheter needle may be slow to retract or fail to retract entirely.
Product
REF: 382633, BD Insyte Autoguard BC Winged, Shielded IV Catheter with Blood Control Technology, 20GA x 1.00 in (1.1x25 mm) 63 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2018-2025·2025-07-02
CDI OneView System BPM Probe temperature sensor measurement inaccuracy
Terumo Cardiovascular Systems is recalling CDI OneView System BPM Probe units due to thermistor assembly errors that cause inaccurate temperature and blood gas measurements, potentially leading to inappropriate clinical decisions.
Product
CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1994-2025·2025-07-02
Barco NexxisOR System Display Encoders and Decoders Recalled
Barco N.V. is recalling certain NexxisOR system display encoder and decoder models due to duplicate MAC addresses that can cause system malfunction, audio/video interruptions, and delayed procedures when multiple units are deployed together.
Product
Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311; MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220; and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; comp
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1996-2025·2025-07-02
DxI 9000 Access Immunoassay Analyzer calibration system error recall
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer C11137 due to calibration issues where curves switch from passed to failed status due to system errors, potentially causing erroneous test results.
Product
DxI 9000 Access Immunoassay Analyzer C11137
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V409000·2025-07-02
Polestar 2 May Lose Brake Function While Using One Pedal Drive
Certain 2021 and 2024 Polestar 2 vehicles may lose brake function while coasting downhill and using One Pedal Drive mode. Polestar will provide a free over-the-air software update to fix the control module defect.
Product
POLESTAR — POLESTAR POLESTAR 2
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2005-2025·2025-07-02
BD Insyte Autoguard Shielded IV Catheter needle retraction malfunction
Becton Dickinson is recalling a specific lot of BD Insyte Autoguard Shielded IV Catheters due to reports that the catheter needle may be slow to retract or fail to retract.
Product
REF: 382544 BD Insyte Autoguard Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2004-2025·2025-07-02
BD Insyte Autoguard BC Pro Winged Shielded IV Catheter Needle Retraction Issue
Becton Dickinson is recalling BD Insyte Autoguard BC Pro Winged Shielded IV Catheters (18 GA x 1.16 in, Lot 4208538) due to reports that the catheter needle may be slow to retract or fail to retract completely.
Product
REF: 381811, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1999-2025·2025-07-02
BD Insyte Autoguard Shielded IV Catheter needle retraction failure recall
Becton Dickinson is recalling BD Insyte Autoguard Shielded IV Catheters (REF 381423, 22GA X 1.00 IN) due to the possibility that the catheter needle may be slow to retract or fail to retract entirely.
Product
REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2007-2025·2025-07-02
BD Insyte Autoguard Shielded IV Catheter needle retraction failure
Becton Dickinson is recalling BD Insyte Autoguard Shielded IV Catheters (20 GA x 1.16 in, REF 381434) because the catheter needle may be slow to retract or fail to retract entirely.
Product
REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2006-2025·2025-07-02
BD Insyte Autoguard Winged Shielded IV Catheter Needle Retraction Issue
Becton Dickinson is recalling BD Insyte Autoguard Winged Shielded IV Catheters (Lot# 4282308) because the catheter needle may be slow to retract or fail to retract entirely following use.
Product
REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07022025-01·2025-07-02
USDA Issues Public Health Alert for Riverbend Ranch Beef Sticks Due to Plastic
USDA FSIS issued a public health alert for Riverbend Ranch beef sticks due to possible plastic contamination. No injuries have been reported.
Product
Top Notch Jerky LLC — FSIS Issues Public Health Alert for Ready-to-eat Beef Jerky Stick Products Due to Possible Extraneous Material Contamination
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1997-2025·2025-07-02
Bigfoot Unity Diabetes Management System Pen Caps Unresponsive Due to Firmware Error
Bigfoot Biomedical is recalling Bigfoot Unity Diabetes Management System Pen Caps due to a firmware issue that may cause insulin pens to become unresponsive. People with diabetes may lack information needed to make timely treatment decisions.
Product
Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release Configuration, Rev H SW-300689-02 Bigfoot Inject v1 Pen Cap RCAP Firmware 1.3.0 Release Configuration, Rev H The Bigfoot Unity Diabetes Management System that include the
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2003-2025·2025-07-02
BD Insyte Autoguard BC Pro IV Catheter Needle Retraction Defect
Becton Dickinson is recalling BD Insyte Autoguard BC Pro Winged Shielded IV Catheters (REF 382944) due to reports that the catheter needle may retract slowly or fail to retract completely.
Product
REF: 382944, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2002-2025·2025-07-02
BD Insyte Autoguard Shielded IV Catheter needle retraction defect
Becton Dickinson is recalling one lot of BD Insyte Autoguard Shielded IV Catheters (REF 381433, 20GA x 1.00 in) due to reports that the catheter needle may retract slowly or fail to retract completely.
Product
REF: 381433, BD Insyte Autoguard Shielded IV Catheter, 20GA x 1.00 in (1.1x25 mm) 65 mL/min, STERILEEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide