The Recall Desk

State

Pennsylvania product recalls

72,969 recalls have nationwide distribution and so reach Pennsylvania. 11,919 additional recalls listed Pennsylvania specifically in their distribution scope.

What the numbers show

Total
11,919
Critical
1,922
Severe
2,866
Most recent
2026-09-16

Of the 11,919 recalls naming Pennsylvania we have scored against our rubric, 1,922 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,866 (24%) are Severe.

Which agencies issued them

These figures cover only the 11,919 recalls whose distribution notice names Pennsylvania specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4726–4750 of 84888

  • CriticalFDA (Food)·H-0156-2026·2025-11-12

    Soft taco dinner kits recalled over an undeclared milk allergen

    Teasdale Foods is recalling 3,654 cases, 21,924 units, of Casa Mamita Soft Taco Dinner Kit sold at ALDI over undeclared milk. The FDA has classified the recall as Class I.

    Product
    Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), UPC: 4099100318715, DIST. & SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL 60510 Product consists of 10 flour tortillas, 1 sauce packet, and 1 seasoning packet within a carton; 6 cartons are packed into a mixed case with 6 addition
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·H-0155-2026·2025-11-12

    Crunchy taco dinner kits recalled over an undeclared milk allergen

    Teasdale Foods is recalling 336 cases, 4,032 units, of Giant/Martin's Crunchy Taco Dinner Kit over undeclared milk. The FDA has classified the recall as Class I.

    Product
    Giant/Martin's Crunchy Taco Dinner Kit, Net Wt 9.4 OZ (266g), UPC: 068826757516, DISTRIBUTED BY: ADUSA DISTRIBUTION, LLC SALISBURY, NC 28147 Product consists of 12 taco shells, 1 sauce packet, and 1 seasoning packet within a carton; packed 12 cartons per case
    Category
    Food
    Distribution
    11 states
  • SevereNHTSA·25V777000·2025-11-12

    Audi SUVs recalled because seat belt buckles may be missing a rivet

    Volkswagen Group of America is recalling certain 2025 Audi Q7, Q8, SQ8 and RS Q8 vehicles because the front seat belt buckles may be missing a rivet that secures the buckle to the stalk.

    Product
    AUDI — AUDI Q8, RS Q8, Q7, SQ8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V776000·2025-11-12

    Winnebago Recalls 2025-2026 Micro Minnie Travel Trailers Due to Fire Risk

    Winnebago is recalling 2025-2026 Micro Minnie travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0158-2026·2025-11-12

    Cooked peeled tail off shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 3,600 cases of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp because the shrimp may be contaminated with Cesium-137.

    Product
    Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp, net wt. 2lbs. UPC 011110626196. Product is packaged in clear plastic bag and has a white label with green stripes on top of each bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0423-2026·2025-11-12

    Curved extension catheter trays 20 cm recalled over header bag seals

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with curved extensions, 12 Fr x 20 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0419-2026·2025-11-12

    Size G hip bearings recalled over commingled implant sizes in packaging

    Zimmer is recalling 63 Dual Mobility Vivacit-E bearings labelled Size G 46 mm because the package contents and label may be commingled with the Size F 44 mm bearing.

    Product
    Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 46 mm O.D., Size G, Bearing, Model/Catalog Number: 110031013; semi constrained hip prosthesis
    Category
    Medical Device
    Distribution
    20 states
  • HighFDA (Food)·H-0163-2026·2025-11-12

    Easy peel deveined shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 1,800 cases of AquaStar 13/15 Raw Shrimp Easy Peel Deveined, sold at Publix, because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0159-2026·2025-11-12

    Raw shrimp skewers recalled over potential Cesium-137 contamination

    AquaStar is recalling 5,220 cases of AquaStar Raw Peeled Tail-on Shrimp Skewers because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. Product is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0161-2026·2025-11-12

    Waterfront Bistro shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 3,600 cases of Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25 because the shrimp may be contaminated with Cesium-137.

    Product
    Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25, net wt. 2lbs., UPC 021130123223. Product was sold at Shaw s and Star Market, Albertson's, Eagle, Carrs-Safeway, and Safeway.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0416-2026·2025-11-12

    Cardiology records system recalled over data saved to the wrong patient

    Spacelabs Healthcare is recalling 142 Sentinel V11 cardiology information systems because patient demographics may default to a previous patient and test data may be saved under another patient's record.

    Product
    Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number: 92810 Software Version: 11.6.0 Product Description: Cardiology Information Management System Component: No The Sentinel Cardiology Information Management System is intended to connect to supported m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0425-2026·2025-11-12

    Straight extension catheter trays 24 cm recalled over header bag seals

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions and IC components, 12 Fr x 24 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0152-2026·2025-11-12

    Clomipramine 25 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 25 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0154-2026·2025-11-12

    Clomipramine 75 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0160-2026·2025-11-12

    Best Yet frozen shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 9,900 cases of Best Yet Frozen Raw EZ-Peel White Shrimp across multiple counts because the shrimp may be contaminated with Cesium-137.

    Product
    Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700282 Best Yet Frozen Raw EZ-Peel White Shrimp 21/25 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700286 Best Yet Frozen Raw EZ-Peel White Shrimp 26/30 (net wt. 1 lbs/pkg; 10
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0155-2026·2025-11-12

    Pain relief caplets recalled because the box names the wrong drug

    Aero Healthcare is recalling two lots of AERO TAB caplets because the outer box states acetaminophen and caffeine while the inner pouch correctly states aspirin and caffeine.

    Product
    AEROTAB PAIN RELIEVER — AEROTAB PAIN RELIEVER (PAIN RELIEVER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0166-2026·2025-11-12

    Strawberry cheesecake ice cream recalled over foil fragments in brown sugar

    Ice Cream Factory is recalling 979 cases and 313 tubs of Strawberry Cheesecake ice cream after aluminum foil and packaging fragments were found in a brown sugar ingredient.

    Product
    Strawberry Cheesecake Ice Cream with graham crackers swirl, 12 oz pack, Single Cup Net Wt: 8.75oz, Case of 12 Strawberry Cheesecake with graham cracker swirl, 2.5-gal Tub, Net Weight 14 pounds Labels read in part as "Ice Cream Factory, Distributed by Ice Cream Factory 1201 Ice C
    Category
    Food
    Distribution
    29 states
  • HighFDA (Devices)·Z-0424-2026·2025-11-12

    Twenty centimetre straight catheter trays recalled over header bag seal integrity

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions, 12 Fr x 20 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0417-2026·2025-11-12

    Dental implant screws recalled because the wrong screw was packaged

    Prismatik Dentalcraft is recalling 208 Inclusive Titanium Screws because an incorrect titanium screw was packaged with the dental implant.

    Product
    Brand Name: Inclusive Product Name: Inclusive Titanium Screw compatible with: Biomet 3i" Certain 3.4/4.1/5.0/6.0 mm Model/Catalog Number: 70-1047-COM0117
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·H-0164-2026·2025-11-12

    Extra large peeled shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 1,458 cases of Publix Extra Large Shrimp Easy to Peel Deveined 21/25 because the shrimp may be contaminated with Cesium-137.

    Product
    Publix Extra Large Shrimp Easy to Peel Deveined 21/25, net wt. 1.5 lbs. UPC 041415064454. Product was sold at Publix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0432-2026·2025-11-12

    Hip bipolar heads recalled over packaging that may compromise sterility

    Total Joint Orthopedics is recalling 103 Klassic BiPolar Heads over a potential packaging issue that could compromise the sterile barrier and present a risk of infection if implanted.

    Product
    Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic BiPolar Head, 41 mm OD, 22 mm Head; 3205.42.022 Klassic BiPolar Head, 42 mm OD, 22 mm Head; 3205.43.022 Klassic BiPolar Head, 43 mm OD, 22 mm Head; 3205.44.028 Klassic BiPolar Head, 44 mm OD, 28 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0420-2026·2025-11-12

    Navigation adapters recalled because the system may miss its specified accuracy

    Integra LifeSciences is recalling 1,198 TruDi Navigation System Multi Instrument Adapters because certain revision combinations may not meet specified accuracy for locating a device in the anatomy.

    Product
    TruDi¿ Navigation System - Multi Instrument Adapter; - Manufacturer's Product Number (Catalog Number): EM-2025-000F Rev 00 or Rev 01;
    Category
    Medical Device
    Distribution
    Distributed nationwide