Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

30551–30575 of 40325

ModerateFDA (Devices)·Z-1263-2016·2016-04-06
Siemens Symbia Gamma Camera Recall for Collimator Change Instructions
Siemens is recalling 726 Symbia gamma camera systems worldwide to provide supplemental instructions clarifying the proper collimator change procedure.
Product
The Symbia gamma camera system Product Usage: The Symbia gamma camera system is a computed tomography x-ray system which is a diagnostic x-ray system intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from the same…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1279-2016·2016-04-06
Philips MultiDiagnost Eleva Foot Switches Recalled for Bent Pedal Defect
Philips Medical Systems is recalling 168 foot switches used with the MultiDiagnost Eleva system because a bent pedal can cause loss of key image functionality.
Product
Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 This Philips MultiDiagnost Eleva is intended to be used as a multifunctional/universal system. General RIF, Fluoroscopy, Radiography and Angiography can be performed along with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1252-2016·2016-04-06
Molteno3 Glaucoma Implants Recalled for Updated Instructions
Innovative Ophthalmic Products is recalling Molteno3 Glaucoma Implants because the package insert was updated to add a caution statement to minimize off-label use.
Product
Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#: M3-175) GL-Single Plate 230mm2 (IOP reorder#: M3-230)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1269-2016·2016-04-06
Beckman Coulter Recalls MicroScan LabPro Software Due to Editing Error
Beckman Coulter is recalling MicroScan LabPro software because it allows incorrect manual editing of carbohydrate substrates for specific test panels.
Product
MicroScan LabPro Information Manager System, Software Versions 1.0 to 4.41 Catalog No. 10638819, 10638820, 10638823, 10638824, 10638825,10638826, 10714149,10714159, 10805072, 10805073, 10975000, 10975001, 6000-0008, 6000-0026. Japan: 10638819 LabPro v4.11 Software Update…
Category
Medical Device
Distribution
3 states
ModerateFDA (Devices)·Z-1268-2016·2016-04-06
Pelton & Crane Recalls Helios Track Mounted Dental Lights
Pelton & Crane is recalling 156 Helios HL3T and HLT track mounted dental lights because they were missing two set screws during initial installation.
Product
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals to illuminate the oral cavity while performing examinations and dental procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1264-2016·2016-04-06
Wfr/aquaplast Recalls Prone Breast Treatment Tables Due to Scale Misalignment
Wfr/aquaplast Corp is recalling 30 prone breast treatment tables and devices because some may have misaligned scales, potentially causing orientation differences.
Product
Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device Product Usage: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Breast Device is a medical charged-particle radiation therapy system. A breast radiation therapy patient…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1285-2016·2016-04-06
Ossur Recalls Knee Shields and Medical Devices Due to Packaging Defect
Ossur Americas is recalling various medical devices, including knee shields and walkers, because the packaging is defective.
Product
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide protection from debris or impact to the patella while a patient participates in motocross activities.
Category
Medical Device
Distribution
48 states
SevereFDA (Devices)·Z-1242-2016·2016-03-30
Siemens IMMULITE 1000 Estradiol Test Recalled for Faslodex Interference
Siemens Healthcare Diagnostics is recalling IMMULITE 1000 Estradiol Test kits because the drug Faslodex may cause falsely elevated results.
Product
IMMULITE 1000 Estradiol Test Code E2 Catalog Number: LKE21, LKE21(D), LKE25 SMN: 10381132, 10702832, 10381142 Product Usage: For in vitro diagnostic use with the IMMULITE¿ and IMMULITE 1000 Analyzers - for the quantitative measurement of estradiol in serum, as an aid in…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1220-2016·2016-03-30
Recall of Bacteria-Contaminated Castile Soap Towelettes in Medical Kits
The FDA is recalling specific lots of Aplicare Castile Soap towelettes found in medical kits due to bacterial contamination.
Product
Covidien Dover PRECSION PRM 14FR SIL FLY Item Code: ¿ PP14SD ¿¿ Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1219-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
Covidien LLC is recalling Castile soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.
Product
Covidien Dover 400 PREM U/M 18FR SLVR FLY Item Code: ¿¿¿ P4P18XSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1230-2016·2016-03-30
Qiagen QFT TB Antigen Tubes Recalled for Potential Endotoxin Contamination
Qiagen is recalling QFT TB Antigen Tubes due to potential endotoxin presence that could cause false positive results in tuberculosis tests.
Product
QFT TB Antigen Tube. QIAGEN Sciences, LLC. The QuantiFERON TB-Gold is an indirect test for M. tuberculosis infection (including disease)
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-1228-2016·2016-03-30
Castile Soap Towelettes Recalled for Bacterial Contamination
FDA is recalling Aplicare Castile Soap towelettes in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover PPREM 18FR UL LTX FOLEY TRY CSD Item Code: P18ULD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1216-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover P400 PREM U/M 18FR SIL FLY Item Code: P4P18SD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1212-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover P400 PREM U/M 16FR SLVR FLY Item Code: P4P16XSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1225-2016·2016-03-30
Castile Soap Towelettes in Medical Kits Recalled for Bacterial Contamination
The FDA is recalling Castile soap towelettes included in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover PREC PRM 16FR SILVER FLY TY Item Code: PP16XSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1211-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Castile soap towelettes used in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover P400 PREM U/M 16FR UL FOLY CSD Item Code:P4P16ULD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1236-2016·2016-03-30
Ambu Aura Gain Laryngeal Masks Recalled for Sterility Assurance Failure
Ambu Inc. is recalling Aura Gain laryngeal masks because damage to the sterile barrier may compromise sterility, risking patient contamination.
Product
Ambu, Aura Gain - Single Use Laryngeal Mask- Sterile for use as an alternative to a face mask for achieving and maintaining control of the airway during routine emergency anesthetic procedures.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1222-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
Aplicare Castile Soap towelettes found in Foley trays and specimen kits are being recalled because they are contaminated with bacteria.
Product
Covidien Dover PRECISION PRM 16FR SIL COUDE CATH SECURE Item Code: PP16CSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1207-2016·2016-03-30
Aplicare Castile Soap Towelettes Recalled Due to Bacterial Contamination
Aplicare Castile Soap towelettes included in Foley Trays and Mid stream specimen kits are being recalled because they are contaminated with bacteria.
Product
Covidien Dover P400 PREM U/M 16FR SIL COUDE CATH SECURE Item Code: P4P16CSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1201-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Castile soap towelettes in Foley trays and midstream kits due to bacterial contamination.
Product
Covidien Dover MIDSTREAM KIT CASTILE SOAP Item Code: 2090SA Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1193-2016·2016-03-30
QiG Group Recalls Algovita Implanted Pulse Generators Due to Connection Issues
QiG Group LLC is recalling 34 Algovita Implanted Pulse Generators because they may fail to connect to external devices unless held very close, preventing reprogramming and recharging.
Product
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1227-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Castile soap towelettes used in Foley trays and specimen kits because they are contaminated with bacteria.
Product
Covidien Dover PRECSION PRM 18FR SIL FLY Item Code: PP18SD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1200-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling 118,400 kits of Castile soap towelettes due to bacterial contamination. The products are used to clean the genital area.
Product
Covidien Dover MIDSTREAM KIT CASTILE SOAP Item Code: 2040SA Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1203-2016·2016-03-30
Recall of Bacteria-Contaminated Castile Soap Towelettes in Medical Kits
FDA is recalling 10,000 units of Aplicare Castile Soap towelettes found in medical kits due to bacterial contamination.
Product
Covidien Dover KIT/STERILE PRESERVE CULT Item Code: 8000SA Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1226-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
Aplicare Castile Soap towelettes included in Foley Trays and Mid stream specimen kits are being recalled because they are contaminated with bacteria.
Product
Covidien Dover PRECISION PRM 18FR SIL COUDE CATH SECURE Item Code: PP18CSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide

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30551–30575 of 40325