The Recall Desk

State

Rhode Island product recalls

73,809 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total
3,054
Critical
221
Severe
708
Most recent
2026-11-04

Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42376–42400 of 76863

  • SevereFDA (Devices)·Z-0059-2018·2017-11-08

    Teleflex Percuvance Percutaneous Surgical System Recalled for Tool Tip Breakage

    Teleflex is recalling specific Percuvance surgical instruments because the tool tip jaws may break, causing fragments to fall off during use.

    Product
    Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Components: (a) 5 mm Atraumatic Johans Grasper, Catalog Number PCVJG5 (b) 5 mm Maryland Dissector, Catalog Number PCVMD5 (c) 5 mm Hem-o-lok Clip Applier, Catalog Number PCVHCA5 (d) 5 mm Traumatic Gripper Grasper…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0065-2018·2017-11-08

    SCA Pharmaceuticals Recalls Oxytocin Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 450 bags of oxyTOCIN 30 units in Lactated Ringers due to a lack of assurance of sterility.

    Product
    oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag, Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0086-44
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0068-2018·2017-11-08

    SCA Pharmaceuticals Recalls Rocuronium Bromide Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 487 syringes of Rocuronium Bromide 10 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    ROCuronium Bromide 10 mg per mL, 5 mL Fill in single dose syringe, (50 mg / 5 mL Total Dose) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-850-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0074-2018·2017-11-08

    Cuttlefish Balls Recalled for Undeclared Milk Allergen

    America New York Ri Wang Food Group Co. Ltd. is recalling cuttlefish balls because they contain undeclared milk. The recall covers multiple package sizes distributed across several US states and Canada.

    Product
    Item# 018 - Cuttle Fish Balls Net Weight: 227g 8 oz (0.5lb) UPC 6 16641 46442 4; 018-5X5 Cuttlefish Balls NETWEIGHT: 25LB (400 OZ) UPC 8 15655 01056 0; Cuttlefish Balls Net Weight: 9 oz (0.56lb) UPC 8 15655 01033 1
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0076-2018·2017-11-08

    Ri Wang Food Group Recalls Fried Fish Tofu for Undeclared Milk

    America New York Ri Wang Food Group Co. Ltd. is recalling specific lots of Fried Fish Tofu because the product contains undeclared milk.

    Product
    Item# 075 - Fried Fish Tofu Net Weight: 227g 8 oz (0.5lb) UPC 6 16641 46454 7; 075-5X5 Fish Tofu NETWEIGHT: 25LB (400 OZ) UPC 8 15655 01040 9; Fish Tofu Net Weight: 9 oz (0.56 lb) UPC 8 15655 01019 5
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0067-2018·2017-11-08

    SCA Pharmaceuticals Recalls Calcium Gluconate Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 76 bags of Calcium Gluconate 2 g in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Calcium GLUCOnate 2 g added to 0.9% Sodium Chloride 50 mL Bag, Each bag contains 9.3 mEq Ca++ Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0510-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0116-2018·2017-11-08

    Tres Latin Foods Recalls Pupusas Due to Undeclared Milk Allergen

    Tres Latin Foods is recalling specific lots of pupusas because they contain undeclared milk, a major food allergen.

    Product
    Tres Latin Foods Pupusas, Stuffed Corn Tortillas with Black Bean & Sweet Corn, Net Wt. 10oz (283g), UPC 85443000237. Keep Frozen [4] 2.5 oz Pupusas. Vegan. Gluten Free. Packaged in carton.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0060-2018·2017-11-08

    SCA Pharmaceuticals Recalls Hydromorphone Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 128 syringes of Hydromorphone HCL 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0078-2018·2017-11-08

    Fish Tofu with Shrimp Filling Recalled for Undeclared Milk

    America New York Ri Wang Food Group Co. Ltd. is recalling Fish Tofu with Shrimp Filling because the product contains undeclared milk.

    Product
    Item# 076 - Fish Tofu with Shrimp Filling Net Weight: 9 oz (0.56 .lb) UPC 8 15655 01025 6; 076-5X5 Fish Tofu with Shrimp NETWEIGHT: 25LB (400 OZ) 8 15655 01065 2; 076 Fish Tofu with Shrimp Net Weight: 227g 8 oz (0.5lb) 6 16641 46455 4
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0115-2018·2017-11-08

    Tres Latin Foods Recalls Pupusas Due to Undeclared Milk Allergen

    Tres Latin Foods is recalling specific lots of Kale & Pinto Bean and Black Bean and Sweet Corn pupusas because they contain undeclared milk.

    Product
    Tres Latin Foods Kale & Pinto Bean pupusas Stuffed Corn Tortillas, Net Wt. 10 oz. (283g), UPC 854430002475, Keep Frozen [4] 2.5 oz Pupusas. Vegan. Gluten Free. Packaged in carton.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0059-2018·2017-11-08

    SCA Pharmaceuticals Recalls Succinylcholine Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 1,248 syringes of Succinylcholine 20 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    SUCcinylcholine 20 mg per mL, Total Volume 10 mL in single-dose syringe, (SUCcinylcholine 200 mg / 10 ml) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0910-29
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0063-2018·2017-11-08

    SCA Pharmaceuticals Recalls Fentanyl and Ropivacaine CADD Cassettes

    SCA Pharmaceuticals is recalling specific lots of fentanyl and ropivacaine CADD cassettes due to a lack of assurance of sterility.

    Product
    fentaNYL as citrate 2 mcg / mL, ROPIVacaine HCl 0.1%, Total Fentanyl Dose (200 mcg per 100 mL) in 0.9% Sodium Chloride single dose CADD Cassette Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0264-64
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·118-2017·2017-11-08

    Nestle Recalls Pork and Beef Hot Pockets for Undeclared Allergens

    Nestle Prepared Foods is recalling approximately 26,400 pounds of frozen pork and beef products because they contain undeclared eggs, milk, soy, and wheat.

    Product
    Nestle Prepared Foods Company Recalls Pork and Beef Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0061-2018·2017-11-08

    SCA Pharmaceuticals Recalls Hydromorphone and Bupivacaine Injection Bags

    SCA Pharmaceuticals is recalling 60 bags of Hydromorphone and Bupivacaine injection due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium Chloride 50 mL (HYDROmorphone Total Dose 1000 mcg) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0331-22
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0069-2018·2017-11-08

    Greencore Recalls Ham Sandwiches for Listeria Contamination Risk

    Greencore USA, LLC is recalling specific ham sandwiches due to potential Listeria monocytogenes contamination. Consumers in seven Northeastern states should check their pantries.

    Product
    (1)Turkey Hill Fresh Selects Ham salad on Homestyle Bread, 4.9 oz (2)American Food and Vending Enza Choice Ham Salad on White Bread, 4.7 oz Packaged in plastic wedge container.
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0066-2018·2017-11-08

    SCA Pharmaceuticals Recalls Phenylephrine Syringes Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 1,221 syringes of Phenylephrine HCl 100 mcg/mL due to a lack of assurance of sterility.

    Product
    PHENYLephrine HCl 100 mcg per mL In 0.9% Sodium Chloride 10 mL Fill Volume in a Single Dose Syringe (1,000 mcg / 10 ml Total Dose), Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR, NDC 70004-0810-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0058-2018·2017-11-08

    A1 Slim Dietary Supplement Recalled for Undeclared Unapproved Drug Ingredients

    Kiriko, LLC. is recalling A1 Slim dietary supplements because FDA analysis found undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine.

    Product
    A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584, www.A1SLIM.COM, [email protected] Bar-Code A105212014
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0064-2018·2017-11-08

    SCA Pharmaceuticals Recalls Morphine Sulfate Due to Sterility Concerns

    SCA Pharmaceuticals is recalling specific lots of morphine sulfate injection due to a lack of assurance of sterility.

    Product
    morphine sulfate 1 mg per mL in 0.9% Sodium Chloride a) Total Volume 100 mL in Single Dose CADD Cassette (Total morphine Dose 100 mg per 100 mL) (NDC 70004-0100-63) b) Total Volume 50 mL in Single Dose Syringe (Total morphine Dose 50 mg / 50 mL) (NDC 70004-0100-22) Rx Only, SCA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0072-2018·2017-11-08

    Hannaford Ham Salad Club Rolls Recalled for Listeria Risk

    Greencore USA is recalling Hannaford Ham Salad Club Rolls due to potential Listeria monocytogenes contamination. The product was sold in several northeastern states.

    Product
    Hannaford Ham Salad Club Roll, 5.1 oz
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Drugs)·D-0062-2018·2017-11-08

    SCA Pharmaceuticals Recalls Fentanyl and Bupivacaine Injection Bags

    SCA Pharmaceuticals is recalling 116 bags of fentanyl and bupivacaine injection due to a lack of assurance of sterility.

    Product
    fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125% (Total FentaNYL Dose 500 mcg/250 mL) in 0.9% Sodium Chloride 250 mL Bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205. NDC 70004-0231-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0086-2018·2017-11-08

    Sid Wainer & Son Dried Chili Peppers Recalled for Undeclared Peanuts

    Sid Wainer & Son is recalling Jansal Valley brand Dried Chili De Arbol Peppers because the product contains undeclared peanuts.

    Product
    Sid Wainer & Son Jansal Valley brand Dried Chili De Arbol Peppers,packaged in a plastic clamshell container 1 ounce size
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0062-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plate

    Smiths Medical ASD Inc. is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., REF 21-7100-24, 100mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps).STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0060-2018·2017-11-08

    Smiths Medical Recalls CADD Medication Cassette Reservoirs with Incorrect Pressure Plates

    Smiths Medical is recalling CADD Medication Cassette Reservoirs because some units may have been manufactured with an incorrect pressure plate.

    Product
    CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included., 50 mL, For use with CADD(R) pumps (except CADD-Micro(TM), CADD-MS(R) 3 and CADD-TPN(R) pumps)., REF 21-7001-24, STERILE EO, Smiths Medical ASD, Inc. For use with CADD(R) pumps…
    Category
    Medical Device
    Distribution
    Distributed nationwide