DrugAug 3, 2022
Lansoprazole Delayed-Release Orally Disintegrating Tablets, 15 mg, 100-count blisters per recall — FDA D-1287-2022
FAILED DISSOLUTION SPECIFICATIONS
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
Latest records
Latest recalls — page 700
The newest recall records with useful source details are listed here.
VehicleJul 28, 2022
Chrysler tail lights recall — NHTSA campaign 22V544000
Chrysler (FCA US, LLC) is recalling certain 2022 Jeep Grand Cherokee and 2021-2022 Jeep Grand Cherokee L vehicles. The tail light side marker assemblies may be damaged and not illuminate.…
tail lightsChrysler (FCA US, LLC)
Medical DeviceJul 27, 2022
Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 recall — FDA Z-1449-2022
Packaging seal integrity not validated resulting in a lack of sterility assurance.
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceJul 27, 2022
AESCULAP S4 Cervical Cross Connector, L26mm, S4C CROSS CONNECTOR FIXED 26MM, product code recall — FDA Z-1445-2022
Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceJul 27, 2022
AESCULAP S4 Cervical Cross Connector L22mm, S4C CROSS CONNECTOR FIXED 22MM, product code recall — FDA Z-1443-2022
Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceJul 27, 2022
Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and recall — FDA Z-1424-2022
Product fails to meet the performance claims quoted on the kit insert: Manual Procedure when calibrating using the standard provided in the kit, the change in absorbance is lower than…
Class IIFDA: TerminatedRandox Laboratories Ltd.
Medical DeviceJul 27, 2022
Becton Dickinson & Company BD Connecta Stopcock with OFF Directed Tap Without Extension Tube recall — FDA Z-1431-2022
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under…
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceJul 27, 2022
Stryker Neurovascular Trevo Trak 21 Microcatheter, REF: 90338 recall — FDA Z-1386-2022
Microcatheter product label on the carton is missing the microcatheter product drawing/illustration.
Class IIFDA: OngoingStryker Neurovascular
Medical DeviceJul 27, 2022
Aesculap Implant Systems ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R recall — FDA Z-1429-2022
Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal fixation system. Redesign of removal…
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceJul 27, 2022
Siemens Medical Solutions USA Sensis Vibe Combo with software version VD12A recall — FDA Z-1426-2022
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJul 27, 2022
Baxter Healthcare Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03 recall — FDA Z-1412-2022
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 27, 2022
Surgical Innovations YelloPort Elite Universal Seal recall — FDA Z-1396-2022
There is the potential that YelloPort Elite Universal Seals packaging may contain small holes which may affect the sterility of the product.
Class IIFDA: CompletedSurgical Innovations Ltd
Medical DeviceJul 27, 2022
Baxter Healthcare Hill-Rom PRO+ MRS Surface For Versacare mattress, REF P3255A02 recall — FDA Z-1414-2022
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 27, 2022
Aesculap Implant Systems ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R recall — FDA Z-1428-2022
Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal fixation system.
Class IIFDA: TerminatedAesculap Implant Systems LLC
Medical DeviceJul 27, 2022
Boston Scientific GreenLight HPSEA Laser Fibers, UPN 0010-2092 recall — FDA Z-1392-2022
Several complaints were received for the affected lot; users received a "Fiber type does not match card type" error message on the GreenLight XPS Laser console, necessitating the…
Class IIIFDA: OngoingBoston Scientific Corporation
Medical DeviceJul 27, 2022
Baxter Healthcare Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01 recall — FDA Z-1415-2022
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 27, 2022
Baxter Healthcare Hill-Rom Centrella Pro+ 36" Surface mattress, REF P7923A03 recall — FDA Z-1416-2022
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceJul 27, 2022
GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000 recall — FDA Z-1427-2022
The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls…
Class IIFDA: OngoingGE Healthcare, LLC
Medical DeviceJul 27, 2022
Becton Dickinson & Company BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) recall — FDA Z-1436-2022
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under…
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceJul 27, 2022
Becton Dickinson & Company BD Connecta Stopcock Without Extension Tube Catalog No. 394605 recall — FDA Z-1435-2022
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under…
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceJul 27, 2022
Becton Dickinson & Company BD Connecta" Plus3 White Blend OEM (sterile, bulk) Catalog No. recall — FDA Z-1439-2022
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under…
Class IIFDA: OngoingBecton Dickinson & Company
Medical DeviceJul 27, 2022
RAYSEARCH LABORATORIES AB RayStation 9B SP1. For radiation treatment planning recall — FDA Z-1403-2022
An issue with propagation of treatment course information from RayStation with RayTreat to RayCare has been identified. During some workflows, information may not be propagated to RayCare.
Class IIFDA: TerminatedRAYSEARCH LABORATORIES AB
Medical DeviceJul 27, 2022
Hobbs Medical Polypectomy Snare, Catalog No. 7202 recall — FDA Z-1388-2022
During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the snare from fully closing, and injury may…
Class IIFDA: OngoingHobbs Medical, Inc.
Medical DeviceJul 27, 2022
Baxter Healthcare Hill-Rom Centrella Pro+ 40" Surface mattress, REF P7923A04 recall — FDA Z-1417-2022
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in…
Class IIFDA: OngoingBaxter Healthcare Corporation
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories