State

Oregon product recalls

73,596 recalls have nationwide distribution and so reach Oregon. 7,533 additional recalls listed Oregon specifically in their distribution scope.

What the numbers show

Total: 7,533
Critical: 873
Severe: 2,131
Most recent: 2026-10-14

Of the 7,533 recalls naming Oregon we have scored against our rubric, 873 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,131 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,533 recalls whose distribution notice names Oregon specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1926–1950 of 81129

ModerateFDA (Drugs)·D-0634-2026·2026-06-24
Cura Hongos clotrimazole cream recalled over manufacturing practice deviations
Cura Hongos Crema Antifungica, clotrimazole 1%, in 2 oz tubes is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 84 tubes affected.
Product
Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 52924 00683 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0639-2026·2026-06-24
Med Pride hydrocortisone cream 16oz tubes recalled over manufacturing deviations
Med Pride Hydrocortisone Cream 1%, 16 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 4,738 tubes are affected.
Product
Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 16oz (454g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 305061.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2446-2026·2026-06-24
Medline C-section packs and recovery kits contain recalled Mastisol adhesive
Medline C-section kits, packs and recovery kits are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kits: C SECTION CDS985505G C SECTION PACK DYNJ68260D C-SECTION DYNJ905094B C-SECTION RECOVERY #2 CDS820091P
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2414-2026·2026-06-24
Medline EBSI kits contain recalled Mastisol liquid adhesive
The Medline EBSI Kit, EBSI1534, is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline EBSI Kit EBSI1534
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0641-2026·2026-06-24
Med Pride triple antibiotic ointment packets recalled over manufacturing deviations
Med Pride Triple Antibiotic Ointment in 0.9 g packets is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 3,006 tubes affected.
Product
Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc (equivalent to 400 units), Neomycin Sulfate 5 mg, Polymixin B 5000 units, 0.9g packets, 144 packets per box, 130g, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 1 03 52410 30253…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0589-2026·2026-06-24
Kerr Insta-Char 25 gram aqueous suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char in an aqueous base, 25 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0633-2026·2026-06-24
Rapidol triple antibiotic first aid ointment recalled over manufacturing deviations
Rapidol Triple Antibiotic First Aid Ointment, 2 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 84 tubes are affected.
Product
Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5,000 units, net wt. 2oz (57g) tubes, Distributed by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 10096 77162 9.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0638-2026·2026-06-24
Med Pride clotrimazole antifungal cream recalled over manufacturing practice deviations
Med Pride 1% Clotrimazole Antifungal Cream, 1 oz tubes, is being recalled because of CGMP deviations observed during an FDA inspection. 5,755 tubes are affected.
Product
Med Pride, 1% Clotrimazole Antifungal Cream, Net Wt. 1oz (28.3g), Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 524103 0244 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2432-2026·2026-06-24
Medline C-section kits contain recalled Mastisol adhesive with cracking tubing
Medline C-Section Kits and Packs are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kits: C-SECTION KIT DYNJ904305J C-SECTION PACK DYNJ69533C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2443-2026·2026-06-24
Medline Port A Cath kits contain recalled Mastisol liquid adhesive
The Medline Port A Cath convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kits: PORT A CATH DYNJ906818A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2426-2026·2026-06-24
Medline pediatric dressing change kits contain recalled Mastisol liquid adhesive
The Medline Kit: Dressing Change Ped is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive whose butyrate tubing may crack.
Product
Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0635-2026·2026-06-24
Med Pride bacitracin zinc packets recalled over manufacturing practice deviations
Med Pride Bacitracin Zinc Ointment, 500 units in 0.9 g packets, is being recalled because of CGMP deviations observed during an FDA inspection. 1,087 tubes affected.
Product
Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets Net Wt 130g, 144 count box, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30352 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2416-2026·2026-06-24
Medline block trays and indwelling nerve blocks contain recalled Mastisol
The Medline Block Tray and Indwelling Nerve Block kit are being recalled because they contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2448-2026·2026-06-24
HarmonyAIR A-Series surgical light heads may show paint delamination
HarmonyAIR A-Series Surgical Lighting Systems are being recalled because of the potential for paint delamination, meaning chipping or peeling, on the light heads. 4,138 units affected.
Product
HarmonyAIR A-Series Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2440-2026·2026-06-24
Medline driveline and port dressing kits contain recalled Mastisol adhesive
The Medline Driveline Management Kit and Port Dressing Change Kit are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING CHANGE KIT EBSI1328A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2450-2026·2026-06-24
ALYON surgical light head intensity control buttons may detach
ALYON Surgical Lighting Systems are being recalled because the plus and minus buttons used to control light intensity on the light heads may detach. 549 units are affected.
Product
ALYON Surgical Lighting System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0601-2026·2026-06-24
Quala Dental benzocaine anesthetic gel bottles may have incomplete seals
Quala Dental Products Topical Anesthetic Gel, 20% benzocaine strawberry flavor, is being recalled because the product may contain bottles with incomplete seals. 150 units affected.
Product
QUALA TOPICAL ANESTHETIC GEL — QUALA TOPICAL ANESTHETIC GEL (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0590-2026·2026-06-24
Kerr Insta-Char aqueous charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char in an aqueous base, 50 grams activated charcoal, is being recalled because the product did not meet Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-202-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2422-2026·2026-06-24
Medline abdominal and bariatric packs contain recalled Mastisol liquid adhesive
Medline convenience kits including abdominal, bariatric and laparoscopic cholecystectomy packs are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2431-2026·2026-06-24
Medline da Vinci and gynaecology laparoscopy kits contain recalled Mastisol
Medline da Vinci, general robotics and gynaecology laparoscopy convenience kits are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2429-2026·2026-06-24
Medline labor and delivery C-section kits contain recalled Mastisol adhesive
The Medline Labor & Delivery C-Section convenience kit is being recalled because it contains a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive.
Product
Medline convenience kit: (82)LABOR & DELIVERY C-SECTION DYNJ907895F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0642-2026·2026-06-24
Med Pride triple antibiotic ointment tubes recalled over manufacturing deviations
Med Pride Triple Antibiotic Ointment in 1 oz tubes is being recalled because of CGMP deviations and deficiencies observed during an FDA inspection. 8,996 tubes are affected.
Product
Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 5 mg, Polymyxin B 5000 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC 3 52410 30255 8.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2460-2026·2026-06-24
directCHECK whole blood control labeled with incorrect performance range
directCHECK ACT-LR whole blood quality control, level 2, is being recalled because the assayed control carries labeling with an incorrect performance range. 6,060 units affected.
Product
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2418-2026·2026-06-24
Medline pacemaker and open heart packs contain recalled Mastisol adhesive
Medline convenience kits including pacemaker, ICD, open heart and pediatric open heart packs are being recalled over a recalled lot of Mastisol Liquid Adhesive.
Product
Medline convenience kits: LOOP PACK DYNJ61460C OPEN HEART CDS840150Y PACEMAKER DYNJ56297C PACEMAKER PK DYNJT3454 PACEMAKER/ICD PACK DYNJ33822L PAD OPEN HEART DYNJ900962O PEDIATRIC OPEN HEART DYNJ54238L DYNJT6766 STAZ BASIC VASCULAR DYNJ909794C…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0591-2026·2026-06-24
Kerr Insta-Char activated charcoal suspension did not meet OTC monograph
VistaPharm Kerr Insta-Char activated charcoal in a sorbitol base with cherry flavor is being recalled because the product did not meet the Over-the-Counter Monograph M023.
Product
VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in 120 mL (4 fl oz), distributed by: VistaPharm, Inc., Largo. FL 33771, NDC 66689-203-04.
Category
Drug
Distribution
Distributed nationwide