State

California product recalls

73,597 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: 1,601
Severe: 3,371
Most recent: 2026-10-21

Of the 13,263 recalls naming California we have scored against our rubric, 1,601 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,371 (25%) are Severe.

Which agencies issued them

These figures cover only the 13,263 recalls whose distribution notice names California specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1876–1900 of 86860

SevereFDA (Devices)·Z-2393-2026·2026-06-24
Arrow PSI catheter kits contain drugs from a recalled supplier
A further group of Arrow PSI kits is being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 72,354 units are affected.
Product
Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU5; PSI KIT: 8.5 FR/ASK-09807-UC; PSI KIT: 9 FR X 4 1/8IN (10 CM)/ASK-09903-HH2; PSI KIT: 9 FR X 10 CM/ASK-09903-LMDTG; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU5; PSI KIT: 9…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2369-2026·2026-06-24
Arrow antimicrobial PSI kits contain drugs from a recalled supplier
Arrow PSI and PSI/CVC kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 348,684 units are affected.
Product
Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU4; PSI/CVC KIT: 9 FR/7 FR X 6IN (16CM)/ASK-09903-AMC1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-CMC1; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU4; PSI…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2394-2026·2026-06-24
Arrow midline catheter kits contain drugs from a recalled supplier
Arrow midline catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 177,014 units are affected.
Product
Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A; AM/AT PI MIDLINE 1L: 4.5FR X 15CM/CDC-41541-MPK1A; AM/AT PI MIDLINE 2L: 5.5FR X 15CM/CDC-41552-MPK1A; AGBA PI MIDLINE 1L: 4.5FR X 15CM/ASK-41541-VFHM; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPK; AGBA PI…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2388-2026·2026-06-24
Arrow hemodialysis and AHDC kits contain recalled supplier drugs
Arrow hemodialysis and AHDC catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 62,719 units affected.
Product
Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3L 12 FR X 16 CM/ASK-12123-UOC1, AHDC KIT: 3-L 12 FR X 16 CM/ASK-12123-UPM, AHDC KIT: 3L 12 FR X 20 CM/ASK-15123-UOC1, AHDC KIT: 3-L 12 FR X 20 CM/ASK-15123-UPM, AHDC KIT: 3-L 12 FR X 16…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2390-2026·2026-06-24
Arrow SAC catheter kits contain drugs from a recalled supplier
Arrow SAC catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall.
Product
Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B; SAC KIT: 18 GA X 12CM W CHG/SAC-01218-C; SAC KIT: 18 GA X 16CM W BIO/SAC-01618-B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2380-2026·2026-06-24
Arrow peritoneal lavage catheter kits contain recalled supplier drugs
The Arrow peritoneal lavage catheter kit, 8 Fr, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 7,560 units affected.
Product
Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2372-2026·2026-06-24
Arrow 14 Fr hemodialysis kit contains drugs from a recalled supplier
The Arrow two-lumen 14 Fr x 20 cm hemodialysis kit is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 1,180 units affected.
Product
Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2378-2026·2026-06-24
Arrow PICC and delta kits contain recalled supplier drugs
Arrow PICC and PICC/Delta kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 3,481 units affected.
Product
Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC; AGBA PICC: 2L 5.5 FR X 45 CM/ASK-44552-ABKB; AGBA PICC/DELTA KIT: 5.5 FR X 55 CM/ASK-45552-MHBV; AGBA PICC: 1L 4.5FR x 55CM w Biopatch/DLX-45541-HPKB; PICC/DELTA KIT: 2L 5.5 FR X 50 CM/ASK-45052-MC; AGBA PI PICC KIT…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2383-2026·2026-06-24
Arrow pacing and PSI kits contain drugs from a recalled supplier
Arrow Pacing/PSI kits, 5 Fr two-lumen, are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 95 units affected.
Product
Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2364-2026·2026-06-24
Arrow access trays and StimuCath kits contain recalled supplier drugs
Arrow access trays and StimuCath safety kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 205,685 units affected.
Product
Description/REF: ACCESS TRAY/ASK-04001-SUH-S; ACCESS TRAY/ASK-04001-VM1; STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS; STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS; STIMUCATH SFTY KIT: 20G CTH, 18Gx8CM NDL/AB-20608-KS; STIMUCATH KIT: 19G CATH, 17G x 9CM…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2360-2026·2026-06-24
Automated Impella Controller software error affects left ventricular support devices
Automated Impella Controllers are being recalled because of a potential software error when used with left ventricular Impella devices. 10,297 units are affected.
Product
Automated Impella Controller (AIC), for use with left heart support blood pump. Labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2385-2026·2026-06-24
Arrow access trays and PSI kits contain recalled supplier drugs
Arrow access trays and PSI kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 426,041 units are affected.
Product
Description/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH; PSI KIT: 9 FR X 10 CM/ASK-09903-PHP1; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-UPA; PSI KIT: 9 FR X…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2363-2026·2026-06-24
Arrow paracentesis kits contain drugs from a recalled supplier
Arrow paracentesis kits, REF AK-00376 and ASK-00376-VCU, are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 50,724 units affected.
Product
PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2395-2026·2026-06-24
Arrow PICC access trays contain drugs from a recalled supplier
The Arrow PICC Access Tray, REF ASK-04001-CG1, is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 360 units affected.
Product
Description/REF: PICC ACCESS TRAY/ASK-04001-CG1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2382-2026·2026-06-24
Arrow drainage and thoracentesis kits contain recalled supplier drugs
Arrow drainage and thoracentesis kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 444,943 units are affected.
Product
Description/REF: DRAINAGE KIT/AK-01600, DRAINAGE KIT/AK-01601, DRAINAGE KIT/ASK-01601-MM, THORACENTESIS KIT/AK-01000-T, THORACENTESIS KIT/AK-01000, THORACENTESIS KIT/ASK-01000-CHP, DRAINAGE KIT/ASK-01000-NW, THORACENTESIS KIT/ASK-01000-UPMS, PNEUMOTHORAX KIT/AK-01500…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2381-2026·2026-06-24
Arrow 12 Fr hemodialysis kit contains drugs from a recalled supplier
The Arrow two-lumen 12 Fr x 16 cm hemodialysis kit is being recalled because it contains lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 1,945 units affected.
Product
Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2366-2026·2026-06-24
Arrow pacing PSI kits contain drugs from a recalled supplier
Arrow Pacing PSI kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 15,915 units are affected.
Product
Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS, PACING PSI KIT: 5 FR 2-L/AI-07155-KS, PACING PSI KIT: 5 FR 2L/ASK-07155-UPM
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2374-2026·2026-06-24
Arrow AHDC catheter kits contain drugs from a recalled supplier
Arrow AHDC three-lumen catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 4,270 units affected.
Product
Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XP1A; AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPN1A; AHDC AGB U-BEND KIT: 2-L 12 FR X 20…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2376-2026·2026-06-24
Arrow central venous catheter kits contain drugs from a recalled supplier
Arrow central venous catheter kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 308,263 units affected.
Product
Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PMAH; 3L PI CVC KIT: 7 FR X 16 CM/ASK-12703-PNM; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PUMH…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2373-2026·2026-06-24
Arrow hemodialysis catheter kits contain drugs from a recalled supplier
Arrow two-lumen hemodialysis kits are being recalled because they contain lidocaine, bupivacaine and 0.9% sodium chloride subject to a supplier recall. 15,425 units affected.
Product
Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F; HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122; HEMODIALYSIS KIT 2L: 14 FR X 15CM AGB/AK-22142-CDC; HEMODIALYSIS KIT 2L: 14 FR X 20CM AGB/AK-25142-CDC; HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UMD…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2465-2026·2026-06-24
ConMed AirSeal 12mm access ports may trigger overpressure alerts
ConMed AirSeal 12 mm Access Ports and Obturators with Blunt Tip are being recalled because of the potential for overpressure alerts. 891 packs, or 5,346 units, are affected.
Product
ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2513-2026·2026-06-24
iLet Bionic Pancreas pumps may become stuck on the lock screen
The iLet Bionic Pancreas is being recalled because a screen unlock failure can leave the user stuck on the Lock Screen, unable to change the cartridge or announce a meal.
Product
iLet Bionic Pancreas, REF: BB1001
Category
Medical Device
Distribution
51 states
HighFDA (Devices)·Z-2483-2026·2026-06-24
Medline 14 Fr coude latex catheters fail performance specifications
Medline Intermittent Latex Coude Catheters pre-connected to a collection bag, 14 Fr, are being recalled across all lots because samples did not meet performance specifications. 8,260 units affected.
Product
MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 14 Fr, 1000mL, Medline Product Number/SKU (REF) URO4RR14C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2514-2026·2026-06-24
BD Connecta stopcock Port C may over thread rather than tightening
BD Connecta BD Luer-Lok 360 stopcocks, REF 394910, are being recalled because the Port C connection may over thread or spin rather than tightening securely. 2,465,500 units affected.
Product
BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or extension tube. The ports can be used to sample blood or for hemodynamic…
Category
Medical Device
Distribution
39 states
HighFDA (Devices)·Z-2515-2026·2026-06-24
Inspire respiratory sensing leads labeled with Use By dates beyond shelf life
Inspire Respiratory Sensing Leads, model 4340, are being recalled because they carry an incorrect Use By Date extending beyond the validated three-year shelf life. 50 units affected.
Product
Brand Name: Inspire Medical Systems, Inc. Product Name: Inspire Respiratory Sensing Lead Model/Catalog Number: 4340 Software Version: N/A Product Description: The Inspire¿ Respiratory Sensing Lead (Model 4340) is designed to detect respiratory effort. The lead features a…
Category
Medical Device
Distribution
Distributed nationwide