FoodOct 19, 2022
WORLDWIDE SEAFOOD PRODUCTS Tidal Seafood Yellowfin Tuna Round Steaks 7 oz MED and LG Best recall — FDA F-0074-2023
Frozen Tuna may contain elevated levels of Histamine
Class IIFDA: TerminatedWORLDWIDE SEAFOOD PRODUCTS LLC
Monthly breakdown
2022 recalls by month
Select a month to review the recall records reported during that period.
December 2022318 records · 4 categoriesNovember 2022270 records · 4 categoriesOctober 2022288 records · 4 categoriesSeptember 2022318 records · 4 categoriesAugust 2022293 records · 4 categoriesJuly 2022334 records · 4 categoriesJune 2022348 records · 4 categoriesMay 2022227 records · 4 categoriesApril 2022205 records · 4 categoriesMarch 2022449 records · 4 categoriesFebruary 2022237 records · 4 categoriesJanuary 2022296 records · 4 categories
2022 recalls — page 31
Records are ordered by the best available source date.
FoodOct 19, 2022
Novis PR, LLC dba Kramer Novis G-PREPROTEIN, Liquid Predigested Protein, Dietary Supplement recall — FDA F-0037-2023
Physical appearance of bottle of G-Pre Protein was atypical. Once opened, unusual odor was noticed and atypical bubbles were present.
Class IIIFDA: TerminatedNovis PR, LLC dba Kramer Novis
FoodOct 19, 2022
Eden Foods 64floz., and 1.82L sizes, all sizes in glass bottle recall — FDA F-0033-2023
culling not performed to remove rotted apples, excessive levels of patulin found in 1 lot
Class IIFDA: TerminatedEden Foods, Inc.
FoodOct 19, 2022
Albertsons Companies Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ recall — FDA F-0034-2023
Undeclared allergen; fish (anchovy)
Class IFDA: TerminatedAlbertsons Companies LLC
FoodOct 19, 2022
Albertsons Companies Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT 12 OZ recall — FDA F-0035-2023
Undeclared allergen; fish (anchovy)
Class IIFDA: TerminatedAlbertsons Companies LLC
VehicleOct 13, 2022
Nissan display function recall — NHTSA campaign 22V772000
Nissan North America, Inc. (Nissan) is recalling certain 2022 Titan, Titan XD, Frontier, and 2021-2022 Rogue vehicles. The in-vehicle infotainment (IVI) system may continuously reboot when…
display functionNissan North America, Inc.
VehicleOct 13, 2022
Jeep Wrangler Plug-In Hybrid Electric (PHEV) traction battery recall — NHTSA campaign 22V768000
Chrysler (FCA US, LLC) is recalling certain 2022-2023 Jeep Wrangler Plug-In Hybrid Electric (PHEV) vehicles. The high voltage (HV) battery pack assembly was built with incorrect fasteners…
traction batteryChrysler (FCA US, LLC)
VehicleOct 13, 2022
Chrysler fuel pump recall — NHTSA campaign 22V767000
Chrysler (FCA US, LLC) is recalling certain 2020-2022 Jeep Wrangler, Ram 1500, and 2021-2022 Jeep Gladiator vehicles equipped with 3.0L diesel engines. The high pressure fuel pump (HPFP)…
fuel pumpChrysler (FCA US, LLC)
VehicleOct 13, 2022
Chrysler pretensioner recall — NHTSA campaign 22V766000
Chrysler (FCA US, LLC) is recalling certain 2022 Ram 1500, Jeep Gladiator, and 2021 Jeep Wrangler vehicles. The front seat belt retractors may have an improperly welded micro gas generator,…
pretensionerChrysler (FCA US, LLC)
Medical DeviceOct 12, 2022
Synthes (USA) Products Hammertoe Continuous Compression Implant (CCI) Kit Part Number recall — FDA Z-0008-2023
Drill Pin (drill bit) is not compatible with the Drill Template included in the kit due to a packaging error, result in a surgical delay and may cause soft tissue damage if a larger…
Class IIFDA: OngoingSynthes (USA) Products LLC
Medical DeviceOct 12, 2022
Wright Medical Technology stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF recall — FDA Z-0005-2023
The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem…
Class IIFDA: OngoingWright Medical Technology, Inc.
Medical DeviceOct 12, 2022
Wright Medical Technology stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF recall — FDA Z-0006-2023
The outer label does not match the device inside the package. The affected lot of EVOLVE Proline Stem 7.5mm +2 contains a size 9.5mm +4 stem, while the affected lot of EVOLVE Proline Stem…
Class IIFDA: OngoingWright Medical Technology, Inc.
Medical DeviceOct 12, 2022
Philips Respironics DreamWear Full Face Mask recall — FDA Z-1781-2022
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceOct 12, 2022
Philips Respironics Therapy Mask 3100 NC/SP recall — FDA Z-1784-2022
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceOct 12, 2022
Hologic The BioZorb LP Marker is an implantable radiopaque marker used to facilitate recall — FDA Z-1858-2022
Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL, contained removable labels with an expiration date that indicated the product had already expired. The expiration date…
Class IIFDA: OngoingHologic, Inc.
Medical DeviceOct 12, 2022
Philips MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a recall — FDA Z-0004-2023
Device may intermittently fail to produce audio. Turning the unit off and on does not resolve the issue; disconnecting and reconnecting to AC power does not reliably resolve the issue.
Class IIFDA: OngoingPhilips North America LLC
Medical DeviceOct 12, 2022
Philips Respironics Amara View Minimal Contact Full-Face Mask recall — FDA Z-1780-2022
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceOct 12, 2022
Philips Respironics DreamWisp Nasal Mask with Over the Nose Cushion recall — FDA Z-1782-2022
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceOct 12, 2022
Philips Respironics Wisp and Wisp Youth Nasal Mask recall — FDA Z-1783-2022
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Class IFDA: OngoingPhilips Respironics, Inc.
Medical DeviceOct 12, 2022
B Braun Medical Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02 recall — FDA Z-0009-2023
Potential for leakage at the catheter hub.
Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceOct 12, 2022
Fresenius Kabi USA Ivenix Infusion System (IIS), LVP Software recall — FDA Z-0002-2023
The display screen may become frozen and unresponsive to user input, triggering an alarm that is evidenced by a buzzer sound and flashing red LEDs as a secondary notification. However, as…
Class IFDA: TerminatedFresenius Kabi USA, LLC
Medical DeviceOct 12, 2022
Zimmer G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 recall — FDA Z-0007-2023
The outer sterile package cavity has a corner wall thickness that is below the specification. The thin corner wall could potentially crack during transit. Potential risks include…
Class IIFDA: OngoingZimmer, Inc.
FoodOct 12, 2022
Renaissance Food Group Seasoned Squash Onion & Dill, NET WT, 10.5 OZ recall — FDA F-0021-2023
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Class IFDA: CompletedRenaissance Food Group
FoodOct 12, 2022
Renaissance Food Group 3 Skewer Veggie Kabobs, NET WT, 1 LB 6 OZ recall — FDA F-0027-2023
Firm received positive test results for L. monocytogenes in a finished product. All products manufactured with the same components are being recalled.
Class IFDA: CompletedRenaissance Food Group
About the 2022 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.