Recently reported

Latest U.S. Recalls

Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.

48,924published records in database
4recall categories represented
Jun 9, 2026newest stored source record
Latest records

Latest recalls — page 56

The newest recall records with useful source details are listed here.

VehicleJun 9, 2026

F-150 headlights recall — NHTSA campaign 26V373000

Ford Motor Company (Ford) is recalling certain 2018-2020 F-150 vehicles previously repaired incorrectly under recall number 20V097. When the headlight switch is turned from "Autolamps" to…

headlightsFord Motor Company
VehicleJun 4, 2026

Chrysler pump recall — NHTSA campaign 26V363000

Chrysler (FCA US, LLC) is recalling certain 2021-2025 Jeep Wrangler, Wrangler 4XE, and Jeep Gladiator vehicles. The electric hydraulic power steering pump wiring may overheat and cause a…

pumpChrysler (FCA US, LLC)
VehicleJun 4, 2026

Honda frame and members recall — NHTSA campaign 26V365000

American Honda Motor Company (Honda) is recalling certain 2016-2022 Honda Pilot, 2017-2023 Ridgeline, 2019-2023 Passport, and 2014-2020 Acura MDX vehicles that were sold in Connecticut,…

frame and membersHonda (American Honda Motor Co.)
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2232-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2231-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2233-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2237-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2235-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2236-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
Medical DeviceJun 3, 2026

Medline kits containing Huons Co recall — FDA Z-2234-2026

Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing…

Class IFDA: OngoingMedline Industries, LP
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