State

West Virginia product recalls

20,364 recalls have nationwide distribution and so reach West Virginia. 0 additional recalls listed West Virginia specifically in their distribution scope.

About recalls in West Virginia

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect West Virginia consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14301–14325 of 20364

SevereFDA (Devices)·Z-0964-2023·2023-02-08
CADD Infusion Administration Sets Recalled for Delivery Failure and Alarms
FDA recalls 726,878 CADD Infusion Administration Sets due to potential tubing occlusion causing delivery failure and false alarm warnings.
Product
CADD Administration Set, List Numbers: a) REF 21-7308-24, b) REF 21-7309-24, c) REF 21-7310-24, d) REF 21-7308-24JP, e) REF 21-7309-24JP. Computerized Ambulatory Delivery Device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0248-2023·2023-02-08
FDA Recalls Easy Care First Aid Kits for Bacterial Contamination
GFA Production's Easy Care First Aid 25 Person kits are being recalled nationwide due to contamination with Bacillus bacteria. The affected first aid cream packets could pose a risk if applied to open wounds.
Product
Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2129
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0963-2023·2023-02-08
CADD Infusion Administration Sets Recalled for Tubing Occlusion and False Alarms
Smiths Medical is recalling CADD Administration Sets for two issues: tubing may become blocked, preventing medication delivery, and devices may show false alerts about disposable attachment status.
Product
CADD Administration Set, List Numbers: 1) REF 21-7300-24, 2) REF 21-7301-24 3) REF 21-7302-24, 4) REF 21-7321-24, 5) REF 21-7322-24, 6) REF 21-7323-24, 7) REF 21-7324-24, 8) REF 21-7333-24, 9) REF 21-7336-24, 10) REF 21-7339-24, 11) REF 21-7343-24, 12) REF 21-7349-24,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0929-2023·2023-02-08
SARS-CoV-2 Antigen Rapid Test Kits Recalled for Lack of FDA Authorization
Universal Meditech Inc. is recalling approximately 56,300 SARS-CoV-2 Antigen Rapid Test Kits distributed without FDA approval, clearance, or Emergency Use Authorization. Products were distributed nationwide in California and Texas.
Product
Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1 KIT Green and white box under the brand DiagnosUS, and, White box without brand name labeled as "SARS -COV-2 ANTIGEN DEVELOPMENT MADE IN USA ORAL SWAB TES
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0247-2023·2023-02-08
FDA Recalls First Aid Cream Packets Over Bacterial Contamination
The FDA is recalling Adventure First Aid 1.5 first aid kits due to bacterial contamination found in the included burn cream packets. The contamination was identified through FDA laboratory testing.
Product
Adventure First Aid 1.5, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0212
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0249-2023·2023-02-08
Easy Care First Aid Kits Recalled for Bacterial Contamination
GFA Production is recalling Easy Care First Aid 10 Person First Aid Kits because the included After Burn Cream packets are contaminated with Bacillus bacteria. Contamination was identified through FDA laboratory testing.
Product
Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2128
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0252-2023·2023-02-08
CVS First Aid Home Burn Cream Packets Recalled for Bacterial Contamination
CVS First Aid Home, First Aid Kit burn cream packets have been recalled due to bacterial contamination. The product contains Bacillus lichenformis and Bacillus sonorensis bacteria, creating a risk when applied to wounds or burns.
Product
CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 2980-0700
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V663000·2023-02-08
Coach House Platinum II recreational vehicle window adhesive failure recall
Coach House is recalling 2019-2022 Platinum II and 2022 Platinum recreational vehicles due to window adhesive failure. The adhesive bonding the window vent may fail, potentially causing detachment and increasing crash or injury risk.
Product
COACH HOUSE — 2021 COACH HOUSE PLATINUM II
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0962-2023·2023-02-08
CADD Administration Set recall: medication underdelivery and false alarms
Smiths Medical is recalling 1.6 million CADD Infusion System Administration Sets due to tubing occlusion causing medication underdelivery and false alarm conditions affecting patients worldwide.
Product
CADD Administration Set, List Numbers: a) REF 21-7346-24; b) REF 21-7363-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1051-2023·2023-02-08
Bard Catheter Repair Kits Recalled for Hardened, Unusable Adhesive
Bard Peripheral Vascular is recalling multiple catheter repair kits because the adhesive may be hardened or coagulated, rendering the kits unusable. Approximately 7,520 units were distributed worldwide.
Product
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter Repair Kit 0601620 6.6F Broviac CV Catheter Repair Kit 0601630 9.6F Hickman CV Catheter Repair Kit 0601680 Hickman / Leonard CV Catheter Repair Kit (all ex
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1028-2023·2023-02-08
Medtronic Perfusion Oxygenator Temperature Monitoring Adapter Detachment Recall
Medtronic has recalled Custom Pack Perfusion Tubing Packs used in cardiopulmonary bypass procedures. The Temperature Monitoring Adapter on the oxygenator may detach during setup or disassembly.
Product
Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF CB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1048-2023·2023-02-08
GORE CARDIOFORM Septal Occluder Recalled for Incomplete Quality Documentation
W L Gore & Associates is recalling 14 units of the GORE CARDIOFORM Septal Occluder (GSX0030A) due to incomplete quality test documentation. The missing verification of device release could pose a potential risk of device failure and serious complications.
Product
GORE CARDIOFORM Septal Occluder, REF: GSX0030A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1023-2023·2023-02-08
Medtronic Affinity Fusion Oxygenator: Temperature Monitoring Adapter May Detach
Medtronic is recalling 2,937 Affinity Fusion Oxygenators used in cardiac surgery because the Temperature Monitoring Adapter may detach during setup or disassembly.
Product
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF BB811. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V540000·2023-02-08
2022-2023 Nova Bus LFS Transit Buses Battery Short Circuit Fire Risk
Nova Bus is recalling certain 2022-2023 LFS transit buses because the high-voltage battery may develop a short circuit due to over-tightened rivnut inserts, creating a fire risk.
Product
NOVA BUS — 2022 NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1035-2023·2023-02-08
Non-sterile procedural knee trays recalled for potential packaging breach
Medline Industries recalls non-sterile Total Knee procedural trays because sterile blades inside can puncture the outer foil packaging. This could compromise sterile blade integrity.
Product
Non-sterile procedural trays labeled as TOTAL KNEE KIT, 1 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1046-2023·2023-02-08
Medline UNITE Foot & Ankle Screw Recalled for Intra-Operative Failure
Medline Industries is recalling 420 units of UNITE FOOT & ANKLE Screws nationwide due to observed intra-operative screw failure when used with specific drill bit sizes. The failure occurs due to excessive torque during surgical insertion.
Product
MEDLINE UNITE FOOT & ANKLE Screw, Polyaxial Locking, Mini T8 (2.0x8mm), REF MMSL2008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1031-2023·2023-02-08
Procedural trays recalled for potential sterile packaging breach
Medline Industries recalls non-sterile procedural trays (LAPAROTOMY CDS) because sterile blades within the kits may puncture the outer foil packaging, compromising sterility.
Product
Non-sterile procedural trays labeled as LAPAROTOMY CDS, 2 per case
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V664000·2023-02-08
2021 Dodge Challenger Safety System Status Indicators May Not Illuminate Properly
2021 Dodge Challenger vehicles may not properly illuminate safety system status indicators in daylight or nighttime conditions. This could prevent drivers from knowing the status of vehicle safety systems, increasing crash risk.
Product
DODGE — 2021 DODGE CHALLENGER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1032-2023·2023-02-08
Non-sterile procedural trays with potential sterile packaging breach
Medline Industries is recalling non-sterile procedural trays containing sterile blades that may damage sterile packaging due to blade puncture risk. Lot 22IBQ980. No illnesses reported.
Product
Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·23115·2023-02-08
Fabuloso Multi-Purpose Cleaners Recalled for Bacterial Contamination Risk
Colgate-Palmolive is recalling about 4.9 million Fabuloso Multi-Purpose Cleaners due to contamination with Pseudomonas bacteria. People with weakened immune systems, external medical devices, or underlying lung conditions face a risk of serious infection from exposure.
Product
Fabuloso Multi-Purpose Cleaners
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V668000·2023-02-08
Land Rover seat belt retractor defect affects child restraint security
Land Rover is recalling certain 2020-2022 vehicles because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly. This can increase the risk of injury during a crash.
Product
LAND ROVER — 2021 LAND ROVER DEFENDER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1030-2023·2023-02-08
Non-sterile procedural trays risk sterile packaging breach
Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.
Product
Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1047-2023·2023-02-08
Medline UNITE Foot & Ankle Drill Bit Recalled for Intra-operative Screw Failure Risk
Medline Industries recalls 190 UNITE foot and ankle drill bits due to observed screw failure during surgery. When used to pre-drill holes for certain screw sizes, the drill bits may fail under surgical torque, creating risk during procedures.
Product
MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core, REF MPN10013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1033-2023·2023-02-08
Non-sterile orthopedic procedural trays recalled for potential sterile packaging breach
Medline Industries recalls non-sterile orthopedic procedural trays that may contain sterile blades capable of puncturing the protective foil packaging, compromising sterile barriers.
Product
Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1026-2023·2023-02-08
Affinity Fusion Oxygenator adapter may loosen during cardiac surgery
Medtronic is recalling Affinity Fusion Oxygenators because the Temperature Monitoring Adapter may come loose during setup or disassembly of the heart-lung machine used in cardiac surgery. No injuries have been reported.
Product
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF CB841. Used in Cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide