State

California product recalls

73,584 recalls have nationwide distribution and so reach California. 13,263 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total: 13,263
Critical: 1,605
Severe: 3,368
Most recent: 2026-10-21

Of the 13,263 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,368 (25%) are Severe.

Which agencies issued them

These figures cover only the 13,263 recalls whose distribution notice names California specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

776–800 of 86847

ModerateFDA (Devices)·Z-3095-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potentially Contaminated Wipes
Cardinal Health 200, LLC is recalling 846 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant, posing a risk of localized skin irritation.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GYN ROBOTIC GSAM , Catalog Number: PBCCGRSGD; 2) KIT, GYN ROBOT ACCESSORY , Catalog Number: PB35GYBJC; 3) KIT, PRIMARY RESECTION , Catalog Number: PGVMOTBB19…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0816-2026·2026-09-09
Baxter Recalls Clindamycin Phosphate Injection Due to CGMP Deviations
Baxter Healthcare is voluntarily recalling Clindamycin Phosphate Injection due to Current Good Manufacturing Practice (CGMP) deviations. The affected product was distributed in the US, Puerto Rico, and Chile.
Product
CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3105-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 44 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, CHONY ORTHO MAJOR SPINE , Catalog Number: POV2SCCPP; 2) KIT,ORTHOPLASTIC MICROVASCULAR, Catalog Number: PWVMFFABLI
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0822-2026·2026-09-09
Bionpharma Recalls Doxylamine Succinate Tablets Due to Foreign Material Presence
Bionpharma Inc. is recalling Doxylamine Succinate and Pyridoxine HCl tablets because foreign tablets or capsules were found in the product.
Product
DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE — DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE (DOXYLAMINE SUCCINATE AND PYRIDOXINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3104-2026·2026-09-09
Cardinal Health Recalls Surgical Kits with Potentially Contaminated Wipes
Cardinal Health is recalling 645 surgical kits containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ASLMC CRANIOTOMY , Catalog Number: PNCGCNAUM; 2) KIT, ORP MAJOR SPINE , Catalog Number: PNHDFSVCI; 3) KIT,ORP NEURO TRAUMA , Catalog Number: PNHDOTVCQ…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3100-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Potentially Contaminated Wipes
Cardinal Health is recalling 61 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ENT HARVEST , Catalog Number: PEVMETBJX; 2) KIT, ENT HARVEST , Catalog Number: PEVMETB37
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3096-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 19 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, LUNG TX CIRCULATOR , Catalog Number: OVC3507231
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3093-2026·2026-09-09
Fresenius Citrasate Liquid Acid Concentrate Recalled for Discoloration
Fresenius Medical Care is recalling Citrasate Liquid Acid Concentrate for Bicarbonate Hemodialysis due to complaints of blue-green discoloration.
Product
Citrasate, Liquid Acid Concentrate for Bicarbonate Hemodialysis: Product Numbers: 08-2251-CA, 08-3251-CA, 13-2251-CA; Liquid Acid Concentrate for Bicarbonate Hemodialysis
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3097-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 115 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,ROBOTICS DH , Catalog Number: PGOCRDNHD; 2) KIT, EAS ROBOTIC , Catalog Number: PG36RPEAB; 3) KIT, VIDEO THORACOSCOPY CMC , Catalog Number: PVCGVTACF
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3098-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Potentially Contaminated Wipes
Cardinal Health is recalling 2,448 urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant, posing a risk of localized skin irritation.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG540; 2) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG542; 3) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG55I…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0825-2026·2026-09-09
Allies Group Recalls Subpotent Sunscreen Gel Due to Inadequate SPF Protection
Allies Group Inc. is recalling specific lots of THE ONE SPF 50 Invisible Sunscreen Gel because testing showed the product may not provide the labeled SPF 50 protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 074733
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0826-2026·2026-09-09
Allies Group Recalls Subpotent SPF 50 Sunscreen Gel
Allies Group Inc. is recalling 2,149 tubes of SPF 50 sunscreen gel because testing showed it may not provide the labeled sun protection.
Product
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 90ml - 3 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC 8 885014 075853
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3047-2026·2026-09-09
Diagnostica Stago Recalls STA Staclot Protein S Reagent Due to QC Drift
Diagnostica Stago is recalling 5,220 units of STA Staclot Protein S reagent because quality control values drifted within the stated stability period.
Product
STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor deficiency test
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3102-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling specific urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM3; 2) KIT, ROBOTIC HYST , Catalog Number: PB41RHRM4; 3) KIT, C SECTION , Catalog Number: PLVMCS22G…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3099-2026·2026-09-09
Cardinal Health Recalls Urinary Catheter Trays with Contaminated Wipes
Cardinal Health is recalling 60 units of urinary catheter trays containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,MAXILLOFACIAL PRESBYTERIAN, Catalog Number: PWV2MF01D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0812-2026·2026-09-09
Baxter Recalls Pantoprazole Sodium Infusion Bags Due to Manufacturing Deviations
Baxter Healthcare is voluntarily recalling specific lots of Pantoprazole Sodium infusion bags due to Current Good Manufacturing Practice (CGMP) deviations.
Product
PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM IN 0.9% SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0830-2026·2026-09-09
Mylan Recalls Mycophenolate Mofetil Injection Due to Dissolution Failures
Mylan Pharmaceuticals is recalling Mycophenolate Mofetil for injection because it failed to meet dissolution specifications.
Product
MYCOPHENOLATE MOFETIL — MYCOPHENOLATE MOFETIL (MYCOPHENOLATE MOFETIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0839-2026·2026-09-09
Mylan Recalls Prasugrel Tablets for Failed Dissolution and Stability Testing
Mylan Pharmaceuticals is recalling 47,662 bottles of Prasugrel 10mg tablets because they failed dissolution specifications and 18-month stability testing.
Product
PRASUGREL — PRASUGREL (PRASUGREL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3094-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potential Lubricant Contamination
Cardinal Health is recalling Presource Packs containing CliniClean Pericare Wipes due to potential lubricant contamination that may cause localized skin effects.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,GYN LAPAROSCOPY DH , Catalog Number: PBOCGLN17
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3101-2026·2026-09-09
Cardinal Health Recalls Presource Packs with Potentially Contaminated Wipes
Cardinal Health 200, LLC is recalling 1,398 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.
Product
Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, BLO ROBOTIC GYN , Catalog Number: PBCGRGB28; 2) KIT , GYN MAJOR BARNES JEWIS, Catalog Number: PBVMLP22G; 3) KIT, GYN OPERATIVE LAPAROSCOPY, Catalog Number: PBVM0722D…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2026·2026-09-09
Sage Products Recalls Chlorhexidine Gluconate Cloth Due to Cross Contamination
Sage Products, LLC is recalling 165,536 packages of 2% Chlorhexidine Gluconate Cloth due to cross-contamination with other products.
Product
CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0833-2026·2026-09-09
Supernus Recalls Trokendi XR Topiramate Capsules for Dissolution Failure
Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) extended-release capsules because they failed dissolution specifications. The recall covers 11,304 bottles distributed nationwide.
Product
Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-102-30.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0840-2026·2026-09-09
Buprenorphine Sublingual Tablets Recalled for Labeling Mix-up
American Health Packaging is recalling 10,953 cartons of Buprenorphine Sublingual Tablets due to a label mix-up. The affected lot is distributed nationwide.
Product
BUPRENORPHINE — BUPRENORPHINE (BUPRENORPHINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-3089-2026·2026-09-09
B Braun Recalls Discofix Stopcock Sets Due to Incorrect Expiration Date
B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the carton shipper labels display an incorrect expiration date.
Product
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V575000·2026-09-07
Can-Am Recalls Motorcycles Due to Instrument Cluster Freezing Risk
Bombardier Recreational Products is recalling specific Can-Am motorcycles because the touchscreen instrument cluster may freeze or go blank, hiding critical safety information.
Product
CAN-AM — CAN-AM SPYDER RT, SPYDER F3, PULSE, ORIGIN
Category
Vehicle
Distribution
Distributed nationwide