State

Oklahoma product recalls

73,722 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,040
Severe: 1,493
Most recent: 2026-10-28

Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29326–29350 of 79544

HighFDA (Devices)·Z-3036-2020·2020-10-07
Ameditech Recalls ImmuTest Drugs of Abuse Cups for Performance Failures
Ameditech is recalling ImmuTest Drugs of Abuse Cups because they failed to consistently detect all compounds at labeled levels.
Product
ImmuTest Drugs of Abuse Cup (AMT Item Number/ AMT Description): IMCA-5AB-W / "ImmuTest Drugs of Abuse Cup AMP1000+BZO300+COC300+OPI2000+THC50 With Cr, Ni, pH, Bl, S.G.", IMC-8BBCE/ "ImmuTest Drugs of Abuse Cup 8 Drug Detection…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3022-2020·2020-10-07
Encore Medical Recalls Humeral Socket Inserts Due to Size Mismatch
Encore Medical is recalling 37 humeral socket inserts because the size etched on the product may differ from the size on the patient sticker label.
Product
RSP Standard HUMERAL SOCKET INSERT, 40 MM plus 4MM, HXe-Plus, Part No. 509-00-440
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-3049-2020·2020-10-07
Ameditech Recalls First Check 4 Panel Drug Cups Due to Performance Failures
Ameditech Inc is recalling 537,120 units of First Check 4 Panel Drug Cups because they may fail to consistently detect all compounds at labeled levels.
Product
First Check 4 Panel Drug Cup: COC/MET1000/OPI2000/THC): (THC/COC); AMT Item Number 990100B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3017-2020·2020-10-07
Olympus BF-Q180 Bronchovideoscope Recalled for Infection Risk and Regulatory Issues
Olympus is recalling BF-Q180 bronchovideoscopes because they lack 510(k) clearance and are associated with a higher rate of patient infections.
Product
Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope Olympus BF Type Q180 (BF-Q180) All serial numbers - Product Usage: designed to be used with an Olympus video system center, light source, documentation equipment, monitor, EndoTherapy accessories (such as…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3037-2020·2020-10-07
Ameditech MicroScreen Immunoassay Recalled for Inconsistent Detection Performance
Ameditech Inc is recalling 23,000 MicroScreen immunoassay units because they failed to consistently detect compounds at labeled levels.
Product
MicroScreen (AMT Item Number/ AMT Description): MSCA-6MBAU/ "MicroScreen AMP300/BZO200/COC300/MET300/OPI300/ THC50 with Cr, Ni, pH, Bl, S.G. "
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1620-2020·2020-10-07
365 Everyday Value Organic Salted Popcorn Recalled for Glass
Eagle Family Foods Group is recalling 365 Everyday Value Organic Classic Salted Popcorn because pieces of glass may be present in the product.
Product
365 Everyday Value Organic Classic Salted Popcorn, 6 oz. bag, UPC 099482435332, 10 retail units per wholesale case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3024-2020·2020-10-07
Office Depot Recalls JINYINSHAN KN95 Masks Due to Filtration Failure
Office Depot is recalling 25,360 JINYINSHAN KN95 masks because test results showed they failed to filter more than 95% of particulates.
Product
JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3021-2020·2020-10-07
Encore Medical Recalls Mislabeled Humeral Socket Inserts
Encore Medical is recalling 15 units of RSP Standard Humeral Socket Inserts due to size labeling discrepancies that could lead to incorrect implantation.
Product
RSP Standard HUMERAL SOCKET INSERT, 44MM, HXe-Plus, Part No. 509-00-044
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-0005-2021·2020-10-07
Endo GIA Auto Suture Universal Loading Unit Recall for Staple Formation Defect
FDA is recalling Endo GIA Auto Suture Universal Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Endo GIA Auto Suture Universal Loading Unit 45 mm - 2.5mm, Item Code 030454 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3038-2020·2020-10-07
Ameditech MicroTox Immunoassay Enzymes Recalled for Performance Failures
Ameditech Inc is recalling MicroTox immunoassay enzymes because they failed to consistently detect compounds at labeled levels.
Product
MicroTox (AMT Item Number/ AMT Description): MTPA-6MBAU / "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G.", MTPA-6MBAU/ "MicroTox (AMP300/BZO200)+(COC300/THC50)+ (MET300/MOR300) With Cr, Ni, pH, Bl, S.G."
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3015-2020·2020-10-07
Stryker IsoAir 2.0 Support Surface Recalled for CPR Connector Defect
Stryker is recalling 110 IsoAir 2.0 support surfaces because a connector defect may delay CPR during cardiac arrest.
Product
Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the microclimate of the patient skin, Model Number: 2941-001-100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1622-2020·2020-10-07
Nature's Promise Organic Lightly Salted Popcorn Recalled for Glass Contamination
Eagle Family Foods Group LLC is recalling Nature's Promise Organic Lightly Salted Popcorn because pieces of glass may be present in the product.
Product
Nature's Promise Organic Lightly Salted Popcorn, 6 oz. bag, UPC 688267142611, 9 retail units per wholesale case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0014-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb sutures that could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" C-12 Cutting, Product Number: SV2294, UDI 20884521151403 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0036-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,272 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. This condition could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" GS-21 Taper CV946, UDI: 20884521151298 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0011-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb sutures because their use could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" P-14 Cutting, Product Number: SV935, UDI: 20884521151755 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0021-2021·2020-10-07
Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,248 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" SC-1, Product Number: SV2239, UDI: 20884521151779 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0001-2021·2020-10-07
Endo GIA Stapler Loading Units Recalled for Staple Formation Defects
FDA recalls Endo GIA Auto Suture Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Endo GIA Auto Suture Gray Universal Articulating Loading Unit 30 mm - 2.0 mm, Item Code 030450 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V620000·2020-10-07
Lance Travel Trailers Recalled for Propane Stove Gas Leak Fire Risk
Lance Camper is recalling certain 2018-2021 travel trailers with Dometic propane stoves that may develop gas leaks, increasing fire risk. No injuries have been reported.
Product
LANCE — LANCE TRAVEL TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0013-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 3,109 units of non-sterile Velosorb sutures distributed nationwide. The defect poses a risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" KV-34 TaperCutting, Product Number: CV919, UDI: 20884521151649 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3046-2020·2020-10-07
Ameditech Recalls First Check 1 Panel Drug Cup Due to Performance Failures
Ameditech Inc is recalling First Check 1 Panel Drug Cup (THC) units because immunoassay enzymes failed performance tests, preventing consistent detection of compounds.
Product
First Check 1 Panel Drug Cup: (THC); AMT Item Number 990400B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0029-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 2,499 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18" P-12 Cut, Product Number: SV496, UDI: 20884521184258 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0039-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling 1,222 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, which could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36" GS-25 CV604, UDI: 20884521152288 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1618-2020·2020-10-07
365 Organic White Cheddar Popcorn Recalled for Glass Contamination
Eagle Family Foods Group LLC is recalling 365 Whole Foods Market Organic White Cheddar Popcorn because pieces of glass may be present in the product.
Product
365 Whole Foods Market Organic White Cheddar Popcorn, 4 oz. bag, UPC 099482428747, 16 retail units per wholesale case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0009-2021·2020-10-07
Recall of Covidien Endo GIA Universal Loading Units Due to Staple Formation Defect
FDA is recalling specific Covidien surgical stapler kits because the staples may not form properly, potentially preventing adequate hemostasis during surgery.
Product
Covidien Best Practices Procedure Kits containing Auto Suture Endo GIA Universal Loading Units, Parent Codes 00Z2760 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0026-2021·2020-10-07
Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures
Riverpoint Medical is recalling non-sterile Velosorb sutures that could compromise the sterile field and increase the risk of surgical site infection.
Product
Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" V-20 Taper, Product Number: CV416G, UDI: 20884521149363 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
Category
Medical Device
Distribution
Distributed nationwide