Summary
The FDA issued a Class II for Hill-Rom Progressa Bed System by Baxter Healthcare Corporation. Reason: The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a max.
Details
Source
Device Recall
External ID
Z-0231-2023
Action Date
2022-11-23
Status
Ongoing
Category
device
Product Description
Hill-Rom Progressa Bed System
Lot/Code Info: UDI/DI 00887761000100, Serial Numbers: X157AW7312, X206AW8017, X154AW7292, X166AW7416, X207AW8041, X158AW7351, X157AW7326, X157AW7313, X206AW8018, X154AW7293, X166AW7418, X167AW7449, X158AW7352, X157AW7328, X174AW7575, X206AW8019, X154AW7296, X167AW7428, X167AW7450, X158AW7353, X157AW7329, X174AW7579, X206AW8021, X154AW7297, X167AW7429, X167AW7451, X158AW7354, X157AW7330, X181AW7722, X206AW8022, X154AW7298, X157AW7308, X166AW7419, X158AW7355, X157AW7332, X181AW7728, X206AW8023, X154AW7300, X157AW7309, X167AW7425, X206AW8010, X158AW7340, X182AW7736, X206AW8024, X168AW7456, X178AW7622, X167AW7427, X206AW8011, X158AW7341, X182AW7737, X206AW8025, X168AW7478, X178AW7623, X159AW7375, X206AW8012, X158AW7342, X207AW8060, X158AW7344, X171AW7495, X178AW7625, X159AW7378, X206AW8020, X158AW7343, X208AW8079, X206AW8026, X171AW7496, X178AW7626, X159AW7380, X158AW7333, X158AW7349, X208AW8082, X206AW8027, X171AW7497, X178AW7627, X216AW8193, X158AW7334, X158AW7359, X208AW8084, X206AW8028, X171AW7498, X178AW7628, X216AW8194, X158AW7336, X159AW7360, X157AW7305, X206AW8029, X172AW7521, X178AW7629, X168AW7468, X158AW7337, X159AW7361, X158AW7348, X206AW8030, X172AW7522, X154AW7288, X168AW7474, X158AW7338, X159AW7364, X164AW7390, X207AW8038, X172AW7531, X154AW7295, X171AW7481, X158AW7356, X159AW7367, X166AW7403, X207AW8039, X172AW7533, X159AW7370, X206AW8032, X158AW7358, X159AW7374, X167AW7433, X207AW8040, X172AW7534, X159AW7371, X207AW8036, X159AW7363, X159AW7383, X167AW7434, X180AW7693, X173AW7536, X174AW7565, X167AW7447, X154AW7302, X159AW7384, X167AW7435, X181AW7714, X173AW7537, X174AW7567, X172AW7528, X157AW7304, X159AW7385, X201AW7935, X181AW7720, X159AW7382, X199AW7872, X172AW7529, X157AW7316, X159AW7386, X201AW7940, X154AW7289, X166AW7405, X158AW7345, X173AW7539, X157AW7317, X159AW7387, X203AW8005, X154AW7294, X166AW7406, X158AW7346, X173AW7540, X157AW7318, X164AW7395, X203AW8006, X164AW7391, X166AW7407, X158AW7347, X173AW7542, X157AW7320, X166AW7396, X207AW8042, X164AW7392, X166AW7411, X154AW7301, X173AW7543, X157AW7321, X166AW7398, X207AW8043, X164AW7388, X166AW7412, X157AW7311, X173AW7545, X157AW7322, X166AW7399, X207AW8044, X164AW7393, X166AW7414, X159AW7365, X173AW7546, X157AW7324, X166AW7410, X207AW8045, X154AW7291, X166AW7415, X159AW7366, X158AW7350, X157AW7325, X154AW7290 ADDITIONAL SERIAL NUMBERS UPDATED 2/14/2023: X140AW7268, X140AW7269, X140AW7270, X140AW7271, X140AW7272, X140AW7253, X140AW7254, X140AW7255, X140AW7256, X140AW7257, X140AW7258, X140AW7259, X140AW7260, X140AW7262, X140AW7263, X139AW7226, X139AW7227, X139AW7228, X139AW7229, X139AW7230, X103AW6603, X103AW6604, X103AW6605, X103AW6606, X103AW6607, X103AW6608, X103AW6609, X103AW6610, X103AW6611, X103AW6612, X103AW6613, X139AW7232, X139AW7234, X139AW7236, X139AW7237, X139AW7238, X139AW7239, X139AW7240, X139AW7241, X139AW7242, X139AW7243, X140AW7245, X140AW7246, X140AW7249, X140AW7250, X140AW7251, X140AW7252, X140AW7273, X140AW7274, X140AW7275, X154AW7280, X139AW7231, X139AW7235, X139AW7244, X140AW7261, X140AW7264, X140AW7265, X140AW7266, X140AW7267
Quantity Affected: 248 beds (Updated)
Reason for Recall
The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.
Distribution
Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, HI, IN, LA, MA, MO, NC, NM, NV, NY, OK, OR, PA, SC. TN, TX, WA, and WI. (UPDATED: States of PA and SC and there was government distribution.) There was no military distribution. Foreign distribution was made to Canada, Qatar, Singapore, and UAE. UPDATE: Saudi Arabia now included.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-10-18
Company
Deerfield, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 171 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Baxter Healthcare Corporation has 310 FDA actions in our database, including 286 recalls and 24 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Baxter Healthcare Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Baxter Healthcare Corporation have FDA actions?
Baxter Healthcare Corporation has 310 FDA actions in our database, including 286 recalls and 24 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0231-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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