State

Washington product recalls

73,809 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total: 8,536
Critical: 865
Severe: 2,405
Most recent: 2026-11-04

Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41901–41925 of 82345

HighFDA (Drugs)·D-0948-2018·2018-07-25
Avella Recalls Heparin Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 40 bags of Heparin 1,000 Units in NS 250mL due to potential leakage that compromises sterility.
Product
HEPARIN 1,000 Units in NS 250mL. (Heparin Sodium, USP 1,000 Units, 0.9% Sodium Chloride, USP 250 mL) Volume: 251 mL. Single dose bag. For: Adventist Medical Center Hanford. By: Avella of Huston, 9265 Kirby Dr., Houston TX, 77054. NDC 42852-747-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2441-2018·2018-07-25
Zeiss UV Disinfection Unit Recalled for Potential Radiation Exposure
Zeiss is recalling 8 UV disinfection units for the Celldiscoverer 7 microscope because a firmware issue may allow the unit to activate outside its housing, exposing users to harmful UV radiation.
Product
Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1656-2018·2018-07-25
Odwalla Superfood Fruit Smoothie Recalled for Potential Metal Fragments
The Coca-Cola Company is recalling Odwalla Superfood fruit smoothies due to the potential for tiny wire metal fragments in the bottles.
Product
Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5 Odwalla Life Food- Canada only - Unit UPC: 000-14054-03125-5 Ingredients: Apple Juice from concentrate, peach and mango purees from concentrate, banana…
Category
Food
Distribution
33 states
HighFDA (Devices)·Z-2507-2018·2018-07-25
Medtronic Tri-Staple 2.0 Reloads Recalled for Missing Sled Component
Medtronic is recalling Tri-Staple 2.0 Black Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling system 60 mm Extra Thick, Item Code SIG60AXT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2454-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling 588 units of Proline Suture Blue 4x18" 5/0 due to a packaging design issue that may allow the needle to perforate the package, posing a risk of injury or infection.
Product
PROLENE SUTURE BLUE 4X18"5/0 DA RB-2 +PLG, D7879
Category
Medical Device
Distribution
25 states
HighFDA (Drugs)·D-0949-2018·2018-07-25
Avella Recalls Hydromorphone Syringes Due to Sterility Concerns
Avella of Deer Valley is recalling 480 single-dose hydromorphone syringes due to potential bag leakage and lack of sterility assurance.
Product
HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg, 0.9% Sodium Chloride (USP) QS 30 mL) Volume: 30mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX. NDC 42852-222-63
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2452-2018·2018-07-25
Ethicon Recalls Certain Proline Sutures Due to Packaging Design Issue
Ethicon is recalling specific Proline sutures because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.
Product
PROLENE SUTURE 30"(75CM) 4-0 BLUE, D7748
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2460-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Proline sutures because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Product
PROLENE SUTURE 4"(10CM) 8-0 BLUE, D9662
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2446-2018·2018-07-25
NewDeal Large QWIX Medical Device Recalled Due to Infection Risk
NewDeal SA is recalling Large QWIX medical devices because their use may cause superficial or deep infections requiring antibiotic treatment or device removal.
Product
Large QWIX, Model Numbers: 111740S, 111745S, 111750S, 111755S, 111760S, 111765S, 111770S, 111775S, 111780S, 111785S, 111790S, 111795S, 111800S, 111805S, 111810S, 111815S, 111820S, 121740S, 121745S, 121750S, 121755S, 121760S, 121765S, 121770S, 121775S, 121780S, 121785S…
Category
Medical Device
Distribution
19 states
HighFDA (Devices)·Z-2455-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue
Ethicon, Inc. is recalling 432 units of Prolene Suture 30" 8-0 Blue (D8292) because the needle may perforate the packaging, posing a risk of injury or infection.
Product
PROLENE SUTURE 30"(75CM) 8-0 BLUE, D8292
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2459-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue
Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.
Product
PROLENE SUTURE 36"(90CM) 4-0 BLUE, D9067
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2451-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue
Ethicon, Inc. is recalling specific Prolene suture products because a packaging design issue allows the needle to perforate the package, posing a risk of injury or infection.
Product
PROLENE SUTURE 4-36" (90CM) 3-0 BLUE, D6416
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2450-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Design Issue
Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing a risk of injury or infection.
Product
PROLENE SUTURE 4-36"(90CM) 4-0 BLUE, D5988
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2465-2018·2018-07-25
Ethicon Recalls PRONOVA Suture Needles Due to Packaging Perforation Risk
Ethicon is recalling specific PRONOVA suture needles because a packaging design issue may allow the needle to perforate the package, posing injury or infection risks.
Product
PRONOVA SUTURE BLUE MONO POLY - SH-1 Taperpoint 1/2C, D10027
Category
Medical Device
Distribution
25 states
HighFDA (Drugs)·D-0930-2018·2018-07-25
Avella Recalls Ephedrine Syringes Due to Potential Sterility Issues
Avella of Deer Valley is recalling specific lots of ePHEDrine 50mg syringes because bags may leak, compromising sterility.
Product
ePHEDrine 50mg, 50 mg/10 mL (5 mg per mL) (Ephedrine Sulfate, USP 50mg in 0.9% Sodium Chloride, USPQS 10mL. 10 mL-Sterile use dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-805-61
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2458-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Proline sutures because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE 24"(60CM) 7-0 BLUE, D8881
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2461-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Prolene suture products because a packaging design issue may allow needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE BLUE 48" 4-0 D/A SH-1, D9746
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2463-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Proline suture products because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Product
PROLENE SUTURE MONO BLUE BV1755 Taperpoint 3/8C, D9995
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2479-2018·2018-07-25
Hitachi Oasis MRI Systems Recalled for Exposed Belt Hazard
Hitachi Medical Systems America Inc is recalling 264 Oasis MRI systems because an exposed stainless steel belt can cause finger cuts.
Product
Hitachi Oasis MRI system Product Usage: Hitachi MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0944-2018·2018-07-25
Avella Recalls Fentanyl and Bupivacaine Cassettes Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 15 cassettes of fentanyl and bupivacaine due to potential bag leakage and lack of sterility assurance.
Product
fentaNYL 3 mcg/mL, 0.1% Bupivacaine, Fentanyl Citrate, USP 750 mcg, Bupivacaine HCL PF, USP, 250 mg, 0.9% Sodium Chloride, USP QS 250 mL. Volume: 250mL. Single dose Cassette. For: Methodist St. John Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2467-2018·2018-07-25
GE Medical Systems Recalls T2100 Microflex Drive Treadmill Units
GE Medical Systems is recalling T2100 Microflex Drive Treadmills because unaddressed spare parts may cause uncontrolled walking belt motion during stress tests.
Product
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Specifically the T210…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2464-2018·2018-07-25
Ethicon Recalls Proline Sutures Due to Packaging Perforation Risk
Ethicon is recalling 372 units of Proline Suture Blue 18" 7-0 because the needle may perforate the packaging, posing a risk of soft tissue injury or infection.
Product
PROLENE SUTURE BLUE 18" 7-0 D/A BV-1, DC631
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2462-2018·2018-07-25
Ethicon Recalls Certain Prolene Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Prolene suture products because a packaging design issue allows needles to perforate the package, posing risks of soft tissue injury or infection.
Product
PROLENE SUTURE 36"(90CM) 3-0 BLU, D9844
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2457-2018·2018-07-25
Ethicon Recalls Prolene Sutures Due to Packaging Perforation Risk
Ethicon is recalling specific Prolene suture units because a packaging design issue allows needles to perforate the package, posing injury and infection risks.
Product
PROLENE SUTURE 24"(60CM) 6-0 BLUE, D8688
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-2316-2018·2018-07-25
Wescam MX-10 Surveillance Laser System Recalled for Ocular Hazard
Wescam Inc is recalling 29 MX-10 surveillance laser systems because the ocular hazard distance is longer than specified, posing a risk of eye exposure.
Product
MX-10 surveillance laser system Product Usage: The expected usage of the product is to facilitate observation and surveillance missions from safe standoff ranges.
Category
Medical Device
Distribution
Distributed nationwide