State

California product recalls

20,371 recalls have nationwide distribution and so reach California. 0 additional recalls listed California specifically in their distribution scope.

About recalls in California

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 California 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.

14976–15000 of 20371

ModerateCPSC·23717·2022-12-15
Crate and Barrel Thornhill Baby Cribs Recalled for Fall Hazard
Crate and Barrel is recalling about 280 Thornhill baby cribs because mattress support pins can become loose or not fit properly, causing the mattress to fall. The firm received six reports of the mattress support pins not fitting correctly or falling out, though no injuries have been reported.
Product
Thornhill Dark Brown and Natural Baby Cribs
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0330-2023·2022-12-14
Sensititre Medical Device Recall: False Antibiotic Susceptibility Test Results
Remel Inc. is recalling Sensititre HPB1 diagnostic plates that may produce false susceptible results for specific bacteria when tested with seven antibiotics. This could lead to inaccurate susceptibility information affecting clinical treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre HPB1, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0339-2023·2022-12-14
CAIRE Liberator 20 Liquid Oxygen System Recalled for Weld Defects
Caire, Inc. is recalling CAIRE Liberator 20 liquid oxygen system units due to weld penetration inconsistencies discovered during an FDA audit. The manufacturing defect affects 3 units.
Product
CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0337-2023·2022-12-14
Liquid Oxygen System Devices Recalled Due to Weld Quality Issues
Caire Inc. is recalling 70 CAIRE Liberator 45 liquid oxygen systems due to inconsistencies in weld penetration on the inner bottle's longitudinal weld seam discovered during an audit.
Product
CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0331-2023·2022-12-14
Medical Diagnostic Plate Recalled for False Antibiotic Susceptibility Test Results
Remel Inc is recalling 588 units of the Sensititre Gram Negative IVD AST diagnostic plate due to false susceptible test results for certain bacteria when tested with specific antibiotics. The defect could lead to incorrect treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre CMC5VGNF, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0335-2023·2022-12-14
Medical Device Recall: Sensititre Test Produces False Antibiotic Susceptibility Results
Remel Inc. is recalling a diagnostic test that may incorrectly report antibiotic susceptibility in certain Gram-negative bacteria. False results could lead to inappropriate antibiotic treatment.
Product
Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0332-2023·2022-12-14
FDA Class I Recall: Thermo Sensititre Gram Negative Diagnostic Test Inaccuracy
Thermo Scientific Sensititre CMC7AFLF Gram Negative diagnostic tests may produce false susceptible results for certain bacteria, potentially leading to ineffective antibiotic treatment decisions. The FDA has classified this as a Class I recall.
Product
Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0329-2023·2022-12-14
Sensititre GN7F Antibiotic Test Plates Recalled for Inaccurate Susceptibility Results
Remel Inc. recalled 8,073 units of Sensititre GN7F antibiotic susceptibility test plates after discovering they may report false results for certain bacteria, potentially leading to incorrect antibiotic treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0336-2023·2022-12-14
Caire Liberator 45 Liquid Oxygen System Recalled for Weld Defects
Caire, Inc. is recalling 10 CAIRE Liberator 45 liquid oxygen system units due to inconsistencies in weld penetration on the inner bottle discovered during an FDA audit.
Product
CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0334-2023·2022-12-14
Sensititre STP6F diagnostic plates may report false antibiotic susceptibility results
Remel's Sensititre STP6F diagnostic plates may produce false susceptible results for Gram-negative bacteria when tested with certain antibiotics, potentially leading to inappropriate treatment decisions.
Product
Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0327-2023·2022-12-14
Thermo Sensititre diagnostic plate recalled for false susceptibility results
Sensititre diagnostic plates may give false antibiotic susceptibility results for certain bacteria species, potentially affecting treatment decisions. The FDA issued a Class I recall for approximately 1,917 units distributed nationwide.
Product
Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0338-2023·2022-12-14
FDA Class I Recall: CAIRE Liberator 30 Liquid Oxygen System Units
Caire, Inc. is recalling five CAIRE Liberator 30 liquid oxygen system units due to weld defects on the inner bottle that could lead to device failure and loss of oxygen supply to dependent patients.
Product
CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0328-2023·2022-12-14
Medical Device Recall: Sensititre GN6F May Report False Antibiotic Susceptibility Results
The FDA recalled Sensititre GN6F Gram Negative antimicrobial susceptibility test plates (2,471 units) because they may report false results indicating bacteria are susceptible to certain antibiotics when they are actually resistant.
Product
Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0333-2023·2022-12-14
Gram-negative antibiotic susceptibility test device recalled for false susceptible results
Sensititre MDRGN3F antibiotic test device may return false susceptible results for certain gram-negative bacteria, risking inappropriate antibiotic treatment. FDA Class I recall issued.
Product
Thermo SCIENTIFIC, Sensititre MDRGN3F, Gram Negative IVD AST
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0423-2023·2022-12-14
Omnipod 5 Controller charging port melting poses minor burn risk
Insulet is recalling Omnipod 5 Controllers where the charging port and cable may melt or deform from excessive heat, potentially causing minor burns if touched and preventing the device from charging.
Product
Omnipod 5 Automated Insulin Delivery System Product catalog numbers: PT-000409: ASM, Omnipod 5, PDM, Programmed PT-000428: Adaptor, Charging, Noetic Nuu N5004L, Horizon PDM, US PT-000429: Cable, Charging, Omnipod 5, Horizon PDM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0416-2023·2022-12-14
Bipolar Surgical Forceps Recalled Due to Missing Instructions for Use
CareFusion 2200 Inc is recalling V. Mueller bipolar forceps (model F-5304) due to missing Instructions for Use content related to power supply interface and cleaning/maintenance procedures.
Product
CareFusion V. Mueller Neuro/Spine TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 0.5MM TIP, ANGLED-UP, FINE OVERALL LENGTH 8-3/4" (225MM), REF F-5304
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0375-2023·2022-12-14
Carefusion Bipolar Forceps Recalled Due to Missing Instructions for Use
Carefusion is recalling 347 units of SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS due to incomplete Instructions for Use. The missing content covers power supply interface and maintenance procedures.
Product
Carefusion V. Mueller" SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP INSULATED, OVERALL LENGTH 7-3/4" (195MM), REF F-1003
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0387-2023·2022-12-14
Bipolar Forceps Recall Due to Incomplete Instructions for Use
BD recalled Carefusion bipolar forceps due to missing Instructions for Use content regarding power supply interface and cleaning/maintenance. Affected units distributed nationwide and internationally.
Product
Carefusion V. Mueller SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIPS, IRRIGATING OVERALL LENGTH 7-3/4" (19.7CM), REF F-1304
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0363-2023·2022-12-14
IgM and IgA Assay Kits Recalled for Test Carryover Risk
Randox Laboratories recalls IgM and IgA immunoturbidimetric assay kits due to carryover contamination that can cause elevated test results when run immediately after Fructosamine tests on RX instruments.
Product
IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in serum and plasma Catalog Number: IM3834
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0355-2023·2022-12-14
Siemens IMMULITE Testosterone Assay Recalled for Measurement Bias
Siemens is recalling two lots of its IMMULITE Total Testosterone Assay due to a confirmed 40% positive measurement bias at higher testosterone levels, which may delay diagnosis and require repeat testing.
Product
IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000 Analyzers for the quantitative measurement of total testosterone in serum and heparinized plasma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0395-2023·2022-12-14
CareFusion Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion 2200 Inc is recalling 4,557 units of V. Mueller ADSON Bipolar Forceps due to incomplete Instructions for Use. The IFU is missing content about power supply interface and cleaning and maintenance instructions.
Product
CareFusion V. Mueller ADSON BIPOLAR FORCEPS 1.0MM TIP, INSULATED OVERALL LENGTH 4-3/4" (120MM), REF F-3015
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0357-2023·2022-12-14
Dover Urethral Catheter Drainage System Recall for Potential Port Blockage
Cardinal Health is recalling Dover closed urethral catheter trays because the drainage bag port may become occluded, preventing urine from draining properly and increasing the risk of urinary retention.
Product
Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code: 3408 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0463-2023·2022-12-14
Philips MR 7700 System Upgrade Recalled Due to Gradient Coil Fire Risk
Philips is recalling the Upgrade to MR 7700 System (Model 782130) because the gradient coil may act as a heat source and produce smoke or fire. Affected units should not be operated until Philips provides further guidance.
Product
Philips Upgrade to MR 7700 System, Model Number 782130
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0458-2023·2022-12-14
Propel Mini Sinus Implant Recalled for Incorrect Product Label Information
Intersect ENT is recalling 611 units of Propel Mini Mometasone Furoate Sinus Implant due to incorrect product identification information on the label. The label displays wrong reference numbers and UDI-DI codes.
Product
Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0382-2023·2022-12-14
Surgical Bipolar Forceps Recalled for Missing Instructions
Carefusion is recalling the V. Mueller Bipolar Forceps Insulated due to missing instructions for power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller"GERALD BIPOLAR FORCEPS INSULATED, 1.0MM TIP OVERALL LENGTH 7" (180MM), REF F-1112
Category
Medical Device
Distribution
Distributed nationwide